← Ireland

S.I. No. 125/2000 - Radiological Protection Act, 1991 (Ionising Radiation) Order, 2000

Obsah (7)Article 24Article 10Article 21Article 9Article 16Article 3Article 11

Act, 1991 (Ionising Radiation) Order, 2000 Skip to content Disclaimer Feedback Helpdesk Gaeilge Léim go dtí an t-ábhar Séanadh Aiseolas Deasc chabhrach English Gaeilge English Produced by the

fice

the Attorney General Táirgthe ag Oifig an Ard-Aighne Home Legislation Acts

the Oireachtas Statutory Instruments Pre-1922 Legislation Constitution External Resources Bills (Houses

the Oireachtas) Iris Oifigiúil /

ficial Gazette Revised Acts (LRC) Classified List

Legislation (LRC) Translations (acts.ie) Translations (Houses

the Oireachtas) Government Publications for Sale EU Law (EUR-Lex) FAQ Disclaimer Feedback Helpdesk Search Baile Reachtaíocht Achtanna an Oireachtais Ionstraimí Reachtúla Reachtaíocht Réamh-1922 Bunreacht Acmhainní Seachtracha Billí (Tithe an Oireachtais) Iris Oifigiúil Achtanna Athbhreithnithe (CAD) (An Coimisiún um Athchóiriú an Dlí) Liosta Rangaithe Reachtaíochta Aistriúcháin (achtanna.

  1. ie)Aistriúcháin (Tithe an Oireachtais) Foilseacháin Rialtais ar Díol Dlí AE (EUR-Lex) CCanna (Ceisteanna Coitianta) Séanadh Aiseolas Deasc chabhrach Cuardach TitleTeideal Year(
  2. s)or rangeBliain nó blianta nó raon TypeCineál All Legislation Acts Statutory Instruments Advanced SearchCuardach Casta HomeBaile Statutory InstrumentsIonstraimí Reachtúla 2000 S.I. No. 125/2000 - Radiological Protection Act, 1991 (Ionising Radiation) Order, 2000 S.I. No. 125/2000 - Radiological Protection Act, 1991 (Ionising Radiation) Order, 2000 AmendmentsLeasuithe CONTENTS Part 1 Citation, Definitions and Scope Article 1. Citation and Commencement Article 2. Interpretation Article 3. Scope Part 2 Regulation

Practices and Work Activities Article 4. Licensing

Practices Article

  1. Exemptions Article
  2. Licensing Procedures Article
  3. Notification

Work Activities Part 3 Justification, Optimisation and Dose Limitation Article

  1. Justification Article
  2. Optimisation, Dose Constraints and Risk Assessment Article
  3. Dose Limitation Article
  4. Special Protection during Pregnancy and Breast Feeding Article
  5. Specially Authorised Exposures Part 4 Estimation

Effective Dose Article 13. Effective Dose Part 5 Protection

Exposed Workers, Apprentices and Students Article

  1. Arrangements in the Workplace Article
  2. Classification

Areas Article

  1. Requirements for Controlled and Supervised Areas Article
  2. Radiation Safety Procedures Article
  3. Classification

Exposed Workers Article

  1. Radiation Protection Adviser Article
  2. Information and Training Article
  3. Monitoring

Working Environments Article 22. Dose Monitoring

Persons Article

  1. Estimated Dose Article
  2. Approval

Dosimetric Services and Radon Measurement Laboratories Article 25. Medical Surveillance

Category A Workers Article 26. Special Medical Surveillance

Exposed Workers Article 27. Operational Protection

Apprentices, Students and Outside Workers Article 28. Control

Radioactive Substances, Nuclear Devices and Irradiating Apparatus Article 29. Duties

Exposed and Outside Workers, Apprentices, Students and Outside Undertakings Part 6 Work Activities involving Natural Radiation Sources Article 30. Identification

work activities involving significant exposure to radon Article

  1. Remedial Measures Article
  2. Identification

work activities involving significant exposure to natural radiation sources other than radon Article 33. Protection

air crew against exposure to cosmic radiation Part 7 Radiation Protection

the Population for Practices in Normal Circumstances Article 34. Protection

the Public Article 35. Estimates

Population Doses Part 8 Intervention and Emergency Preparedness Article

  1. Intervention Principles Article
  2. Intervention Preparation and Plans Article
  3. Dealing with Radiological Emergencies Article
  4. Emergency Occupational Exposure Article
  5. Intervention in Cases

Lasting Exposure Part 9 Notifications, Notices and Revocations Article

  1. Notifications Article
  2. Enforcement Notices Article
  3. Revocation Schedules to Order Schedule 1 Information to be provided in a licence application for a practice or notification

a work activity Schedule 2 Dose limits for exposed workers, apprentices, students and members

the public Schedule 3 Information to be contained in a health record Schedule 4 Particulars to be contained in a radiation passbook Schedule 5 Annex I

Council Directive 96/29/Euratom Schedule 6 Annex II

Council Directive 96/29/Euratom Schedule 7 Annex III

Council Directive 96/29/Euratom S.I. No. 125

2000 RADIOLOGICAL PROTECTION ACT, 1991 (IONISING RADIATION) ORDER, 2000 I, JOE JACOB, Minister

State at the Department

Public Enterprise. in exercise

the powers conferred on me by subsections

(1)and
(2)

section 30

the Radiological Protection Act. 1991 (No.9

1991), and the Public Enterprise (Delegation

Ministerial Functions) Order, 1998 (No. 16

1998), and for the purposes, amongst other things,

giving effect to Council Directive 96/29/Euratom1

13 May 1996 laying down basic safety standards for the protection

the health

workers and the general public against the dangers arising from ionising radiation and Council Directive 90/641/Euratom2

4 December 1990 on the operational protection

outside workers exposed to the risk

ionising radiation during their activities in controlled areas and after consultation with the Ministers for Finance, Enterprise, Trade and Employment, Agriculture, Food, and Rural Development, Health and Children, Education and Science, Foreign Affairs, the Environment and Local Government, Defence, Marine and Natural Resources and the Radiological Protection Institute

Ireland, hereby order as follows: Part 1 CITATION, DEFINITIONS AND SCOPE 1. Citation and Commencement

(1)This Order may be cited as the Radiological Protection Act, 1991 (Ionising Radiation) Order, 2000.
(2)This Order shall come into operation on 13 May 2000. 2. Interpretation
(1)In this Order- “absorbed dose” or “D” means the energy absorbed per unit mass averaged over a tissue or organ, calculated in accordance with following formula (expressed in grays): D = d ε ____ dm where — d ε is the mean energy imparted by ionising radiation to the matter in a volume element, and — dm is the mass

the matter in this volume element; — d ε is the mean energy imparted by ionising radiation to the matter in a volume element, and — dm is the mass

the matter in this volume element: “accelerator” means apparatus or installation, in which particles are accelerated, emitting ionising radiation with an energy higher than 1 mega-electron volt (MeV); “accidental exposure” means an exposure

individuals as a result

an accident but does not include an emergency exposure: “activation” means a process through which a stable nuclide is transformed into a radionuclide by irradiating with particles or high-energy gamma rays the material in which it is contained; “activity” or “A” means the activity, A.

an amount

a radionuclide in a particular energy state at a given time, calculated in accordance with the following formula (expressed in becquerels): A = dN ____ dt where dN is the expectation value

the number

spontaneous nuclear transitions from that energy state in the time interval dt; “air crew” means the cabin and flight crew

an aircraft operated by an air operator or an undertaking in the State which operates an aircraft; “air operator” means the holder

an Air Operator's Certificate issued by the Irish Aviation Authority in accordance with the Irish Aviation Authority (Air Operators' Certificate) Order, 1999 ( S.I. No. 420

1999 ); “Annex I” means Annex I

the Council Directive (which for convenience

reference is set out in Schedule 5); “Annex II” means Annex II

the Council Directive (which for convenience

reference is set out in Schedule 6); “Annex III” means Annex III

the Council Directive (which for convenience

reference is set out in Schedule 7); “apprentice” means a person receiving training or instruction within an undertaking with a view to exercising a specific skill: “approved dosimetric service” means a body that carries out - (a) the calibration, reading or interpretation

individual monitoring devices, or (b) the measurement

radioactivity in the human body or in biological samples, or (c) the assessment

doses. being a body which is referred to in subparagraph (a) or (b)

Article 24

(1); “approved medical practitioner” has the meaning assigned to it by Article 25
(2); “approved radon measurement laboratory” means a laboratory that carries out - (a) the calibration, reading or interpretation

radon detectors, (b) the measurement

radon concentration in air, or (c) the assessments

doses due to radon. being a body which is referred to in subparagraph (a) or (b)

Article 24

(1); “artificial sources” means radiation sources other than natural radiation sources; “category A worker” means an exposed worker designated as such pursuant to Article 18
(1); “category B worker” means an exposed worker designated as such pursuant to Article 18
(2); “committed effective dose” or “E(t)” means the sum

the committed organ or tissue equivalent doses (H r τ) resulting from an intake, each multiplied by the appropriate tissue weighting factor WT and is calculated in accordance with the following formula (expressed in sieverts): E(τ) = ΣwT HT (τ) T where in specifying E(τ), τ is given in the number

years over which the integration is made; “committed equivalent dose” or “HT (τ)” means the integral over time (t)

the equivalent dose rate in tissue or organ T that will be received by an individual as a result

an intake and is calculated in accordance with the following formula (expressed in sieverts): t0 + τ HT(τ) = ∫ HT (t)dt t0 for an intake at time t0 where - Hτ (t) is the relevant equivalent dose rate in organ or tissue T at time t, - τ is the time, expressed in years, over which the integration is performed or where τ is not specified, a period

50 years is assumed for adults and up to age 70 for children; “controlled area” means an area classified as such under Article 15: “Council Directive” means Council Directive 96/29/Euratom

13 May 1996, laying down basic safety standards for the protection

the health

workers and the general public against the dangers arising from ionising radiation; “disposal” means, in relation to waste - (a) the emplacement

waste in a repository, or a given location, without the intention

retrieval, or (b) the approved direct discharge

wastes into the environment, with subsecuent dispersion; “dose constraint” means a restriction on the prospective dose to individuals which may result from a defined source, for use at the planning stage in radiation protection whenever optimisation is involved; “dose limits” means maximum values laid down in Schedule 2 for the doses resulting from the exposure

workers, apprentices and students and members

the public to ionising radiation to which this Order applies, being the values

the sum

the relevant doses from external exposures in the specified period and the 50 year committed doses (up to age 70 for children) from intakes in the same period; “effective dose” or “E” means the sum

the weighted equivalent doses in all the tissues and organs

the body specified in Schedule 6 from internal and external radiation and is calculated in accordance with the following formula (expressed in sieverts): E = ΣwT HT = Σ wT Σ wR DT.R T T R where - DT.R is the absorbed dose averaged over tissue or organ T, due to radiation R, - WR is the radiation weighting factor, - WT is the tissue weighting factor for tissue or organ T, and - the appropriate WT and WR values are specified in Schedule 6; “emergency exposure” means an exposure

individuals who are implementing the necessary rapid action to bring help to endangered individuals, prevent exposure

a large number

people or save a valuable installation or goods, whereby any one

the individual dose limits specified in Schedule 2 could be exceeded; “equivalent dose” or “HT.R” means the absorbed dose in tissue or organ T, weighted for the type and quality

radiation R. and calculated in accordance with the following formula (expressed in sieverts): HT.R = wR DT.R where - DT.R is the absorbed dose averaged over tissue or organ T. due to radiation R. and - wR is the radiation weighting factor, the appropriate values

which are specified in Schedule 6; “exposed workers” means persons, either self-employed or working for an employer, who are subject to an exposure incurred at work from practices or work activities to which this Order applies, being an exposure liable to result in doses exceeding one or other

the dose levels equal to the dose limits for members

the public; “exposure” means the process

being exposed to ionising radiation; “functions” includes powers and duties and a reference to the performance

functions includes with respect to the powers and duties, a reference to the exercise

the powers and the carrying out

the duties; “health detriment” means an estimate

the risk

reduction in length and quality

life occurring in a population following exposure to ionising radiation, (including such a reduction in length or quality arising from somatic effects, cancer and severe genetic disorder); “High Radon Area” means an area where the Institute predicts that more than 10%

dwellings in that area will have radon concentrations above 200 Bq m-3 or such other area as the Institute may determine from time to time; “Institute” means the Radiological Protection Institute

Ireland; “intake” means the activities

radionuclides entering the body from the external environment; “intervention” means a human activity that prevents or decreases the exposure

individuals to radiation from sources which are not part

a practice or which are out

control, by acting on sources, transmission pathways and individuals themselves; “intervention level” means a value

avertable equivalent dose, avertable effective dose or a derived value, at which the taking

intervention measures should be considered; the avertable dose or derived value is solely that associated with the exposure pathway to which the intervention measure is to be applied; “ionising radiation” means the transfer

energy in the form

particles or electromagnetic waves

a wavelength

100 nanometers or less, or a frequency

3 x 1015 Hertz or more, capable

producing ions directly or indirectly; “irradiating apparatus” means an apparatus capable

producing ionising radiation and containing components operating at a potential difference

more than 5kV; “licence” means a licence referred to in section 30

the Principal Act; “medical exposure” means (a) the exposure

patients as part

their own medical diagnosis or treatment, (b) the exposure

individuals as part

occupational health surveillance, (c) the exposure

individuals as part

health screening programmes, (d) the exposure

healthy individuals or patients voluntarily participating in medical or biomedical, diagnostic or therapeutic, research programmes, or (e) the exposure

individuals as part

medico-legal procedures; “Member State” means a Member State

the European Communities; “members

the public” means individuals in the population, excluding exposed workers, apprentices and students during their working hours and individuals or volunteers during the exposures referred to in subparagraphs (a), (b) and (c)

Article 10

(3); “Minister” means the Minister for Public Enterprise; “National Accreditation Board” means the committee

that name established by resolution

the Board

Forfas, pursuant to section 10

the Industrial Development Act, 1993 (No. 19

1993), as amended by section 46

the Industrial Development (Enterprise Ireland) Act, 1998 (No. 34

1998); “natural radiation sources” means sources

ionising radiation from natural terrestrial or cosmic origin; “nuclear device” means any machine or apparatus the operation

which involves the use

a radioactive substance, an irradiating apparatus or a nuclear reactor; “outside undertaking” means the employer

an outside worker; “outside worker” means a Category A worker who carries out services in the controlled area

any undertaking (other than in the controlled area

his or her own undertaking or his or her employer's undertaking), whether self-employed or an employee

an outside undertaking, including such an undertaking which has its principal place

business in another Member State; “population” means the whole population including exposed workers, workers, apprentices, students and members

the public; “potential exposure” means an exposure, that is not expected to be delivered with certainty, with a probability

occurrence that can be estimated in advance; “practice” means a human activity that can increase the exposure

individuals to radiation from an artificial source, or from a natural radiation source where natural radionuclides are processed for their radioactive, fissile or fertile properties, other than an activity that results in an emergency exposure; “Principal Act” means the Radiological Protection Act, 1991 (No. 9

1991); “radiation passbook” means - (a) in the case

an outside worker whether self-employed or employed in the State by an outside undertaking, a passbook approved for the purposes

this Order by the Institute; (b) in the case

an outside worker employed in another Member State by an outside undertaking, a passbook authorised by the competent authority

that Member State; “radiation protection adviser” shall be construed in accordance with Article 19

(3); “radioactive contamination” means the contamination

any material, surface or environment or

an individual by radioactive substances and, in the case

the human body, includes both external skin contamination and internal contamination, irrespective

route

intake; “radioactive substance” means any substance capable

emitting ionising radiation and includes any radionuclide, whether natural or artificial; “radiological emergency” means a situation that requires urgent action in order to protect workers, members

the public or the population, either partially or as a whole; “radon” means radon-222 gas in air; “reference group

the population” means a group comprising individuals whose exposure to a source is reasonably uniform and representative

that

the individuals in the population who are the more highly exposed to that source; “registered medical practitioner” has the meaning assigned to it by the Medical Practitioners Act 1978 , (No. 4

1978); “sealed source” means a source whose structure is such as to prevent, under normal conditions

use, any dispersion

the radioactive substances into the environment; “source” means an apparatus, a radioactive substance or an installation capable

emitting ionising radiation or radioactive substances; “supervised area” means an area classified as such pursuant to Article 15; “total equivalent dose” or “(HT)” means the sum

the equivalent doses due to a radiation field which is composed

types and qualities

radiation with different values

WR and is calculated in accordance with the following formula (expressed in sieverts): HT = ΣwR DT.R R where - DT.R is the absorbed dose averaged over tissue or organ T. due to radiation R. and - wR is the radiation weighting factor, the appropriate values

which are specified in Schedule 6; “undertaking” means any natural or legal person who, as a self employed person or employer as the case may be, carries on or intends to carry on any practice or work activity to which this Order applies, and references to “the undertaking” are to the particular undertaking carrying on the practice or work activity concerned: “workplace” includes any place, land or other location at, in, upon or near which, work is carried on whether occasionally or otherwise and, in particular, includes - (a) a premises, including a cave or mine, (b) an installation on land and any

fshore installation (including any

fshore installation to which the Principal Act applies), (

  1. c)a tent, a temporary structure or movable structure, and (
  2. d)a vehicle, vessel or aircraft.

(2)A word or expression that is used in this Order and is also used in the Council Directive shall, unless the contrary intention appears, have the same meaning that it has in the Council Directive.
(3)In this Order (other than in Schedule 5, 6 or 7) - (a) a reference to an Article or Schedule is a reference to an Article

or Schedule to this Order unless it is indicated that a reference to some other enactment is intended; (b) a reference to a paragraph or subparagraph is a reference to a paragraph or subparagraph

the provision in which the reference occurs unless it is indicated that reference to some other provision is intended. Scope 3.

(1)This Order applies to all practices which involve a risk from ionising radiation emanating from an artificial source or from a natural radiation source in cases where natural radionuclides are being or have been processed in view

their radioactive, fissile or fertile properties including - (a) the custody, production, processing, handling, holding, storage, use. manufacture, importing into or exporting from the European Union, distribution, transportation, recycling, re-use or other disposal

radioactive substances and nuclear devices and, without prejudice to the generality

the foregoing, includes - (i) the operation and decommissioning

any facility involved in the nuclear fuel cycle and the exploitation and closure

uranium mining, (ii) the deliberate addition

radioactive substances in the production and manufacture

medicinal products and the import or export

medicinal products to which radioactive substances have been deliberately added, (iii) the deliberate addition

radioactive substances in the production and manufacture

consumer goods and the import or export

consumer goods to which radioactive substances have been deliberately added, (iv) the deliberate administration

radioactive substances to persons and, in so far as radiation protection

human beings is concerned, animals for the purpose

medical or veterinary diagnosis, treatment or research, (v) the use

radioactive substances for industrial radiography or processing

products, or research, or the exposure

persons for medical diagnosis or treatment. (b) the custody, distribution or use

irradiating apparatus including x-ray sets for industrial radiography, or the processing

products or research or the exposure

persons for medical diagnosis or treatment and the use

accelerators excluding electron microscopes; (c) any other practice specified by the Institute.

(2)Save where otherwise indicated in this Order, this Order also applies to work activities not referred to in paragraph
(1)which - (a) take place in workplaces having radon concentrations in excess

400 Bq m-3, averaged over a minimum period

3 months, or (b) involve natural radiation sources, other than radon, which result in an effective dose to workers or members

the public in excess

1 mSv in a period

12 months.

(3)Articles 7, 11, 33 and 42

this Order apply to work activities involving the operation

aircraft pursuant to an Air Operator's Certificate whereby any member

the air crew is liable to be subject to exposure to cosmic radiation in excess

1 mSv in a period

12 months.

(4)Articles 15, 16, 17, 29
(1)(a) and 34
(3)do not apply where the persons concerned are undergoing medical exposure.
(5)In accordance with Articles 36 to 40, this Order also applies to any intervention in cases

radiological emergencies or in cases

lasting exposure resulting from the after effects

a radiological emergency or a past or old practice or work activity.

(6)This Order does not apply to exposure to radon in dwellings, to the natural level

radiation arising from radionuclides contained in the human body, to cosmic radiation prevailing at ground level or to above ground exposure to radionuclides present in the undisturbed earth's crust. Part 2 REGULATION

PRACTICES AND WORK ACTIVITIES Licensing

Practices 4.

(1)Subject to Article 5, a practice to which this Order applies shall not be carried on save under and in accordance with a licence issued by the Institute.
(2)Such a licence shall not be granted in respect

the deliberate addition

radioactive substances in the production

foodstuffs, toys, personal ornaments and cosmetics and the import and export

such goods. Exemptions 5.

(1)Subject to paragraph
(2), Article 4 does not apply to practices involving - (a) radioactive substances where the quantities involved do not exceed in total the exemption values set out in column 2

Table A to Annex I or in exceptional circumstances, different values authorised by the Institute that satisfy the criteria in Annex I, (b) radioactive substances where the concentrations

radioactivity per unit mass do not exceed the exemption values set out in column 3

Table A to Annex I or, in exceptional circumstances, different values authorised by the Institute that satisfy the criteria set out in Annex I, (

  1. c)apparatus containing radioactive substances exceeding the quantities or concentration values specified in paragraph (
  2. a)or (b), provided that - (
  3. i)it is

a type approved by the Institute, (ii) it is constructed in the form

a sealed source, (iii) it does not cause, in normal operating conditions, a dose rate exceeding 1 uSvh-1 at a distance

0.1 m from any accessible surface

the apparatus, and (

  1. iv)conditions for disposal have been specified by the Institute, (
  2. d)the use

any electrical apparatus to which this Order applies, other than that referred to in subparagraph (e), provided that - (i) it is

a type approved by the Institute, and (ii) it does not cause, in normal operating conditions, a dose rate exceeding 1 uSvh-1 at a distance

0.1 m from any accessible surface

the apparatus, or (e) the use

any cathode ray tube intended for the display

visual images, or other electrical apparatus operating at a potential difference not exceeding 30 kV, provided that this operation does not cause, in normal operating conditions, a dose rate exceeding 1 uSvh-1 at a distance

0.1 m from any accessible surface

the apparatus;

(2)Nothing in paragraph
(1)shall affect the application

this Order to - (a) the deliberate addition

radioactive substances in the production and manufacture

medicinal products and the import or export

such goods, (b) the deliberate addition

radioactive substances in the production and manufacture

consumer goods and the import or export

such goods, (c) the deliberate administration

radioactive substances to persons and, in so far as radiation protection

human beings is concerned, animals for the purpose

medical or veterinary diagnosis, treatment or research, or (d) the disposal, recycling or reuse

radioactive substances or radioactive materials arising from any licensed practice. Licensing Procedures 6.

(1)An application for a licence shall be made to the Institute not later than one month before the proposed commencement

the practice concerned.

(2)An application for a licence shall be in such form as the Institute determines and shall include - (
  1. a)the particulars specified in Schedule 1, (
  2. b)the risk assessment for the proposed practice referred to in Article 9
(2), and (c) the radiation safety procedures referred to in Article 17
(1),
(3)In the case

a practice for which justification in accordance with Article 8 is required, an application for a licence in respect

the practice shall also include a statement setting out grounds for the justification

the practice.

(4)Where in the opinion

the Institute the information supplied by an applicant in an application is insufficient or inadequate for the purpose

enabling the Institute to decide whether or not to grant a licence, it may by notice in writing (sent to the applicant at the address specified in the application) require the applicant to furnish the Institute with such additional information as it specifies in the notice.

(5)A licence shall, subject to any condition relating to expiry specified in the licence, expire on the date specified in that behalf in the licence.
(6)Where the holder

a licence proposes to apply for a further licence to operate from the expiry

his or her existing licence, he or she shall apply to the Institute in accordance with the provisions

paragraph

(2)for such further licence not later than 1 month before the expiry

the existing licence. Such an application shall be in such form and contain such particulars as the Institute specifies.

(7)The holder

a licence may at any time before the expiry

the licence apply to the Institute in writing for an amendment to the licence. An application for such an amendment shall - (

  1. a)specify the reasons for the proposed amendment, and (
  2. b)as appropriate, furnish a revised risk assessment and revised radiation safety procedures.

(8)When a licence has been granted, no modifications to practices, equipment or facilities, the subject

that licence, shall be carried out without the prior consent

the Institute.

(9)A licence granted under the Radiological Protection Act, 1991 (General Control

Radioactive Substances, Nuclear Devices and Irradiating Apparatus) Order. 1993 ( S.I. No. 151

1993 ) which is in force immediately before the commencement

this Order shall continue in force in accordance with its terms as if it were a licence granted under this Order and may be amended or revoked accordingly. Notification

Work Activities 7.

(1)This Article applies to a work activity referred to in Article 3
(2)or 3
(3).
(2)The undertaking concerned shall notify the Institute forthwith after the date referred to in paragraph
(3)

the work activity or as provided for in Articles 30

(4)or 32
(3)and shall provide it with the information concerning the work activity referred to in Schedule 1.
(3)The date referred to in paragraph
(2)is - (a) in case the work activity commenced before the commencement

this Order. the commencement

this Order, and (b) in case the work activity commenced after such commencement, the commencement

the work activity.

(4)Where, in the opinion

the Institute, the information supplied by an undertaking in accordance with paragraph

(2)is insufficient or inadequate, the Institute may, by notice in writing, require that undertaking to furnish the Institute with such additional information as it specifies in the notice.
(5)Where an undertaking has notified the Institute

a work activity in accordance with paragraph

(2)and subsequently makes a material change in that work activity which would affect the information so notified, the undertaking shall forthwith notify the Institute

that change. Part 3 JUSTIFICATION, OPTIMISATION AND DOSE LIMITATION Justification 8.

(1)No practice shall be licensed under this Order unless- (a) it falls within a class or type

practice carried on immediately before the commencement

this Order, or (b) it falls within a class or type

practice which has been approved in writing by the Institute (which the Institute is hereby empowered to do) as being justified by its economic, social or other benefits in relation to the health detriment it may cause.

(2)If an undertaking wishes to apply for a licence to carry on a practice

a class or type not carried on immediately before the commencement

this Order or already approved in writing by the Institute, then it must submit with its application, in accordance with Article 6

(3), the grounds on which it believes the proposed practice is justified by its economic, social or other benefits in relation to the health detriment it may cause.
(3)If the Institute considers that the grounds submitted under paragraph
(2)do not provide justification for the proposed practice, it shall afford the undertaking an opportunity to make further representations in relation to the matter.
(4)If the Institute considers, in the light

new and important evidence about the efficacy or consequences

any practice, that the carrying on

the practice is no longer justified, it shall give notice in writing to any undertaking holding a licence to carry on the practice that it proposes to revoke that licence pursuant to its powers under the Principal Act.

(5)If the Institute proposes to revoke a licence in the circumstances referred to in paragraph
(4), it shall by notice in writing (sent to the applicant at the address specified in his or her application under Article 6) inform the applicant

that proposal and invite him or her to make representations to the Institute, within 1 month from the date

the giving

the notice, as to why, in this applicant's opinion, the licence ought not to be revoked. Optimisation, Dose Constraints and Risk Assessment 9.

(1)The undertaking shall ensure that all exposures, including those to the population as a whole, from practices and work activities under its control, are kept as low as reasonably achievable, taking into account economic and social factors, except for - (a) the case

medical exposures other than radiotherapeutic procedures, which exposures shall be kept as low as reasonably achievable consistent with obtaining the required diagnostic information, taking into account economic and social factors, and (b) the case

medical exposure

individuals for radiotherapeutic purposes, in which exposures

target volumes shall be individually planned, taking into account that doses to non-target volumes and tissues shall be as low as reasonably achievable and consistent with the intended radiotherapeutic purpose

the exposure.

(2)For the purpose

identifying the protective measures needed to restrict exposures to ionising radiation, the undertaking shall, before commencing a practice, make an assessment acceptable to the Institute

the risks

exposure to ionising radiation arising from the practice or from reasonably foreseeable accidents resulting from the practice for workers and members

the public who may be affected.

(3)The undertaking shall, in respect

a work activity, make an assessment acceptable to the Institute

the risks

exposure to ionising radiation arising from the work activity to any workers or members

the public for the purposes

identifying the protective measures needed to restrict exposure to ionising radiation.

(4)Where, in the opinion

the Institute, the assessment provided by the undertaking in accordance with paragraph

(2)or
(3)is insufficient or inadequate, the Institute may, by notice in writing sent to the undertaking at the address specified in its application under Article 6 in the case

a practice, or at the address given in its notification under Article 7, in the case

a work activity require that undertaking to furnish the Institute with such additional information as it specifies in the notice.

(5)The undertaking shall, where appropriate, use dose constraints in restricting exposure to ionising radiation pursuant to paragraph
(1). Dose Limitation 10.
(1)Subject to paragraph 2

Schedule 2 persons under 18 years

age may not be assigned to any work which would result in their being exposed workers.

(2)Without prejudice to Article 12, the undertaking shall ensure that each person referred to in Schedule 2 is not exposed to ionising radiation in excess

the dose limit specified in that Schedule in relation to that person in a period

12 months.

(3)Paragraph
(2)does not apply to - (a) the exposure

individuals as part

their own medical diagnosis or treatment, (b) exposure

individuals knowingly and willingly helping (other than as part

their occupation) in the support and comfort

patients undergoing medical diagnosis or treatment, (c) exposure

volunteers participating in medical and biomedical research programmes.

(4)In relation to subparagraphs (b) and (c)

paragraph

(3), the undertaking shall comply with such guidelines as the Institute may issue in relation to the appropriate procedures to be followed in respect

persons exposed in accordance with either

these subparagraphs (and such guidelines may include dose constraints). Special Protection During Pregnancy and Breast Feeding 11.

(1)As soon as may be after a pregnant woman worker informs the undertaking

her condition, the undertaking shall provide a level

protection for the child to be born which is comparable with that provided for members

the public.

(2)The undertaking shall ensure that the conditions for the pregnant woman in her employment after she has so informed it

that matter are such that the equivalent dose to the child to be born is as low as reasonably achievable and will be unlikely to exceed 1 mSv during the remainder

the pregnancy following the undertaking being informed

the pregnancy.

(3)On being informed by a woman that she is breast feeding, the undertaking shall not employ her in work involving a significant risk

bodily radioactive contamination. Specially Authorised Exposures 12.

(1)In exceptional circumstances, excluding radiological emergencies and evaluated on a case by case basis, the Institute may, where some specific operation so requires, authorise under this Article individual occupational exposures

particular workers exceeding the dose limits specified in Schedule 2 but only if such exposures are limited in time, confined to certain working areas and are within maximum exposure levels defined for the particular case by the Institute.

(2)The undertaking shall submit an application to the Institute carefully justifying the proposed exposure and providing information about the risks involved and precautions to be taken.
(3)The undertaking shall permit only Category A workers who have volunteered for such exposures to be subject to exposures authorised under this Article.
(4)Apprentices, students, pregnant women and breast-feeding women shall not be permitted to be subject to such exposures.
(5)Before an exposure authorised under this Article takes place, the undertaking shall consult with the workers concerned, the approved medical practitioner and the radiation protection adviser.
(6)The undertaking shall ensure that information about the risks involved and the precautions to be taken during such an exposure are provided to the relevant workers in advance.
(7)The undertaking shall ensure that all doses relating to such exposures are separately recorded in the health record referred to in Article 25
(11)and in the individual dose record referred to in Article 22
(2).
(8)An undertaking shall not, without the agreement

the worker, exclude a worker from his usual employment on the grounds that the worker has exceeded a dose limit as a result

an exposure authorised under this Article. Part 4 ESTIMATION

EFFECTIVE DOSE Effective Dose 13.

(1)For the purposes

the estimation

effective and equivalent doses, the values and relationships referred to in Annexes II and III shall be used unless the Institute has authorised the use

equivalent methods.

(2)Without prejudice to paragraph
(1)- (
  1. a)for external radiation, the values and relationships referred to in Annex II shall be used to estimate the relevant effective and equivalent doses, (
  2. b)for internal exposure from a radionuclide or from a mixture

radionuclides, the values and relationships referred to in Annexes II and III shall be used to estimate the effective doses. Part 5 PROTECTION

EXPOSED WORKERS, APPRENTICES AND STUDENTS Arrangements in the workplace 14.

(1)For the purposes

radiation protection, the undertaking shall make arrangements for all workplaces where there is a possibility

exposure to ionising radiation in excess

dose limits specified in paragraph 3

Schedule 2. Such arrangements must be appropriate to the nature

the installations and sources and to the magnitude and nature

the risks. The scope

the precautions and monitoring, as well as their type and quality, must be appropriate to the risks associated with the work involving exposure to ionising radiation. Classification

Areas 15.

(1)The undertaking shall, having regard to the assessment made by it under Article 9
(2), classify as a controlled area any area under its control in which- (a) it is necessary for any person who enters or works in the area to follow a specified system

work designed to restrict exposure to ionising radiation or prevent or limit the probability and magnitude

radiological accidents or their effects, or (b) any person working in the area is liable to receive an equivalent dose greater than 6 mSv in a period

12 months or an equivalent dose greater than three tenths

any relevant dose limit specified in paragraph 1

(2)

Schedule 2, in respect

an exposed worker.

(2)The undertaking shall classify as a supervised area any area under its control, not being classified as a controlled area, in which- (a) it is necessary to keep the conditions

the area under review to determine whether the area should be designated as a controlled area, or (b) any person working in the area is liable to receive an effective dose greater than 1 mSv in a period

12 months or an equivalent dose greater than one tenth

any relevant dose limit specified in paragraph 1

(2)

Schedule 2, in respect

a member

the public.

(3)The undertaking shall keep under review the working conditions in controlled and supervised areas and, if appropriate, revise the classification

the areas concerned. Requirements for Controlled and Supervised Areas 16.

(1)The undertaking shall ensure in the case

a controlled area that - (

  1. a)the area is delineated, (
  2. b)access is restricted to individuals who have received appropriate instructions and is controlled in accordance with the radiation safety procedures. (
  3. c)any outside worker entering or remaining in the area has been certified fit to be classified as a Category A worker in accordance with Article 25, has been issued with the necessary personal protective equipment and is subject to individual dose monitoring pursuant to Article 22, (
  4. d)wherever there is a significant risk

the spread

radioactive contamination, specific arrangements are made including arrangements for the access and exit

individuals and goods. (e) taking into account the nature and extent

the radiological risks in the controlled area, radiological surveillance

the working environment is organised in accordance with Article 21, and (f) signs indicating that it is a controlled area and the nature

the radiological sources and their inherent risks are displayed.

(2)The undertaking shall ensure in the case

a supervised area that - (a) as a minimum, taking into account the nature and extent

the radiological risks in the supervised area, radiological surveillance

the working environment is organised in accordance with the provisions

Article 21

, and (b) if appropriate, signs indicating that it is a supervised area and the nature

the sources and their inherent risks are displayed.

(3)The undertaking, in fulfilling its obligations under paragraphs
(1)and
(2), shall consult with the radiation protection adviser.
(4)The undertaking shall ensure that, in relation to an outside worker, as soon as is reasonably practicable after the services carried out by that outside worker in any controlled area designated by it are completed, an estimate

the dose received by that worker is entered into his or her radiation passbook. Radiation Safety Procedures 17.

(1)For the purpose

enabling work involving ionising radiation to be carried out in accordance with the requirements

this Order and, in particular, for the purpose

identifying the manner in which the safety, health and welfare

workers and other persons shall be secured, the undertaking shall, in respect

any controlled area or, where appropriate having regard to the nature

the work carried out there, any supervised area, prepare a statement in writing

such procedures (in this Order referred to as “radiation safety procedures”) as it considers ought to be followed.

(2)Such a statement shall have regard to the radiological risks involved and the nature

the activities concerned and, in particular, to the assessments carried out under paragraphs

(2)and
(3)

Article 9by the undertaking.

(3)The radiation safety procedures shall be reviewed by the undertaking - (
  1. a)periodically, and (
  2. b)if circumstances arise in which it has reason to believe any

the procedures are no longer appropriate, immediately upon those circumstances arising. and shall be amended by it as it considers appropriate.

(4)When the Institute or an inspector is satisfied that any radiation safety procedures are inadequate in a material way, it may give a direction to the undertaking concerned to amend the procedures in a specified manner and the undertaking shall comply with the direction within 30 days from the date

the direction being given by the Institute.

(5)The undertaking shall take all reasonable steps to ensure that the provisions

the radiation safety procedures prepared by it are observed.

(6)The undertaking shall ensure that the radiation safety procedures prepared by it are brought to the attention

and made available to the workers concerned and other persons who may be affected by them. Classification

Exposed Workers. 18.

(1)The undertaking shall classify as a Category A worker an exposed worker who is liable to receive an effective dose greater than 6 mSv in a period

12 months or an equivalent dose greater than three tenths

the dose limits for the lens

the eye, or, as the case may be, the skin, hands, forearms, feet and ankles specified in paragraph 1

Schedule 2.

(2)The undertaking shall classify as a Category B worker, an exposed worker who is not classified as a Category A worker. Radiation Protection Adviser 19.
(1)The undertaking shall be responsible for assessing and implementing arrangements for the radiological protection

exposed workers.

(2)The undertaking shall appoint in writing one or more suitable persons to perform the functions expressed by this Order to be performable by a radiation protection adviser and a reference in this Article to a suitable person shall be construed as a reference to a person having the knowledge and training needed to carry out physical, technical or radiochemical tests enabling doses to be assessed and to give advice in order to ensure effective protection

individuals and the correct operation

protective equipment.

(3)References in this Order to “the radiation protection adviser” shall be construed as references to the person or, as the case may be, each person so appointed.
(4)The undertaking shall consult with each person so appointed in relation to the steps it takes to comply with this Order.
(5)The undertaking shall not appoint a person to act as a radiation protection adviser unless that person's name appears in the part

the register referred to in paragraph

(6)containing the names

persons for the time being standing approved by the Institute as persons who may be appointed to act as such advisers in relation to the type

practice or work activity concerned.

(6)The Institute shall establish and maintain a register containing the names

persons for the time being standing approved by the Institute as persons who may be appointed to act as radiation protection advisers.

(7)The Institute may approve persons for that purpose whether in relation to practices or work activities generally or a particular type

practice or work activity and the register referred to in paragraph

(6)shall be divided into parts corresponding to those types

practice or work activity (including practices or work activities generally) and the name

each person standing approved under paragraph

(6)shall be entered in the appropriate part

that register accordingly.

(8)For the purposes

paragraph

(6), the Institute may, after consultation with such professional bodies as it considers appropriate, determine and publish educational, training or other requirements (whether relating to qualifications or otherwise) compliance with which it determines to be necessary before it approves a person under that paragraph and different such requirements may be determined with respect to different types

practice or work activity.

(9)Without prejudice to paragraph
(4), the undertaking shall consult the radiation protection adviser in relation to the following matters - (a) the examination and testing

protective devices and measuring instruments, (b) the prior critical examination

plans for installations from the point

view

radiation protection, (c) the acceptance into service

new or modified sources from the point

view

radiation protection, (d) the regular calibration

measuring instruments and the regular checking that they are serviceable and correctly used, (e) the implementation

the requirements

paragraphs

(1)and
(2)

Article 16

. (

  1. f)appropriate quality assurance programmes including quality control measures to be taken under this Order for irradiating apparatus, nuclear devices and radioactive substances, and (
  2. g)the estimation

doses pursuant to Article 23.

(10)The undertaking shall provide the radiation protection adviser with adequate information and facilities for the discharge

his or her functions.

(11)The undertaking shall notify the Institute in writing

the appointment

a radiation protection adviser within 1 month following the date

the appointment.

(12)In this Article “appoint” means to engage - (a) under a contract

service, or (b) under a contract for services, whether whole time or part time and the decision as to which

those methods is used shall be made by the undertaking having regard to the nature

the practice or work activity carried on by it. Information and Training 20.

(1)The undertaking shall inform exposed workers, apprentices and students in relation to - (
  1. a)the health risks involved in their work including - (
  2. i)the general radiation protection procedures and precautions to be taken and, in particular, those involved with operational and working conditions in respect

both the practice in general and each type

work station or job to which they may be assigned, and (ii) the importance

complying with the requirements

this Order, and (b) in the case

women, the need for early declaration

pregnancy in view

the risks

exposure for the child to be born and the risk

contaminating the nursing infant in the case

bodily radioactive contamination.

(2)The undertaking shall ensure that sufficient and appropriate training in the field

radiation protection is provided for exposed workers, apprentices and students.

(3)The undertaking shall ensure that adequate information is given to other persons who are directly concerned with the work with ionising radiation that is carried on by the undertaking to ensure their health and safety so far as is reasonably practicable. Monitoring

Working Environments 21.

(1)The radiological surveillance referred to in Articles 16
(1)(e) and 16
(2)(
  1. a)shall comprise, where appropriate - (
  2. a)the measurement

external dose rates, indicating the nature and quality

the radiation in question, (b) the measurement

air activity concentration and surface density

radioactive substances, indicating their nature and their physical and chemical states, and (c) the measurement

radon by an approved radon measurement laboratory.

(2)The undertaking shall provide suitable and sufficient measuring instruments for carrying out the surveillance referred to in paragraphs
(1)(a) and
(1)(b) and shall ensure that the instruments are properly maintained and fit for the intended purpose. It shall consult the radiation protection adviser with regard to the suitability

the measuring instruments.

(3)The undertaking shall ensure that - (
  1. a)all measuring instruments are individually calibrated before first use and annually thereafter using sources or equipment traceable to appropriate national standards, and (
  2. b)the maintenance, examination and calibration

measuring instruments are carried out by persons who have knowledge

and understanding

currently accepted testing standards and relevant technical guidance in relation to the types

monitoring equipment.

(4)The results

the measurement referred to in paragraph

(1)shall be used, if necessary, for estimating individual doses as provided for in Article 23.
(5)The undertaking shall - (a) make suitable records

the results

the measurements referred to in paragraph

(1)and

the maintenance and calibrations carried out in accordance with paragraph

(3), (
  1. b)ensure that the records made pursuant to subparagraph (
  2. a)are made available to the radiation protection adviser if he or she requests them, and (
  3. c)maintain each

the records referred to in subparagraph (a) for a period

at least 5 years from the date on which it is made. Dose Monitoring

Persons 22.

(1)The undertaking shall ensure that - (
  1. a)individual dose monitoring is carried out by an approved dosimetric service or, as appropriate, by an approved radon measurement laboratory, for all exposed workers, apprentices and students, (
  2. b)in cases where Category A workers are liable to receive significant internal contamination, an adequate system for monitoring is set up; in identifying such cases, the undertaking shall take account

any general guidelines issued by the Institute in that regard, (c) in cases

accidental exposure, the relevant doses and their distribution in the body are assessed, and (d) in cases

emergency exposure, individual monitoring or assessment

the individual doses is carried out as appropriate to the circumstances.

(2)The undertaking shall ensure that - (a) a record containing the results

the individual monitoring is made for each exposed worker, apprentice and student, (

  1. b)the record referred to in subparagraph (
  2. a)contains - (
  3. i)a record

the individual doses measured or estimated, as the case may be, pursuant to paragraph

(1)(a) and Article 23
(1), (ii) in the case

accidental or emergency exposures, the reports

the circumstances and the actions taken, (iii) in the case

specially authorised exposures, a record

the individual doses measured, and (iv) the results

monitoring

the working environment used to assess individual doses, where necessary. (c) the Institute is provided with the summaries

all dose records relating to that year within 3 months

the end

each year; the format

such summaries shall have regard to such guidelines as may be issued by the Institute for the purposes

this Order in that regard, (d) the Institute is notified immediately

any dose received by an exposed worker, apprentice or student in excess

a dose limit specified in paragraphs 1 or 2, as the case may be

Schedule 2, and (e) in the case

Category B workers, the dose record referred to in subparagraph (a) is maintained for at least 5 years from the date on which the measurement was made.

(3)The undertaking shall make suitable arrangements with an approved dosimetric service or radon measurement laboratory, as appropriate, for that service or laboratory - (a) to make assessments

the doses referred to in paragraph

(1)(a) by the use

suitable individual measurements for appropriate periods or where individual measurement is inappropriate, by means

suitable measurements. (b) in the case

Category A workers, to make, keep up to date and maintain a record

the dose assessments referred to in subparagraph (

  1. a)relating to each exposed worker until - (
  2. i)that worker has or would have attained 75 years

age, or (ii) the expiry

the period

50 years from the date on which that worker has ceased to do the work involving exposures, whichever is the later, (c) to provide the undertaking at appropriate intervals with the results

the measurements made in accordance with subparagraph (a), (d) to notify immediately the undertaking and the Institute

any dose received by any exposed worker, apprentice or student in excess

a dose limit specified in paragraphs 1 or 2 as the case may be

Schedule 2.

(4)The undertaking shall provide the approved dosimetric service or radon measurement laboratory with such information concerning its exposed workers, apprentices or students as is necessary for the approved dosimetric service or radon measurement laboratory to comply with the arrangements made for the purpose

paragraph

(3).
(5)If a Category A worker ceases employment with an undertaking, the undertaking by which he or she was employed shall ensure that a copy

the worker's dose records for the previous 12 months is forwarded to the Institute within 3 months

that cessation.

(6)The undertaking shall, at the request

any exposed worker employed by it (whether under a contract

service or a contract for services) or

a person formerly so employed by it, obtain from the approved dosimetric service or radon measurement laboratory and make available forthwith to that worker a copy

the dose record provided for the purposes

paragraph

(2)(a) in respect

that worker.

(7)In the case

an accidental or emergency exposure, the undertaking shall ensure that the results

individual monitoring are submitted to the Institute without delay.

(8)The undertaking shall - (
  1. a)ensure that each outside worker retained by it is provided with an individual radiation passbook which shall be non-transferrable and in which there shall be entered the particulars specified in Schedule 4; and (
  2. b)make suitable arrangements to ensure that the particulars entered in the radiation passbook are kept up-to-date while the outside worker is retained by that undertaking. Estimated Dose 23.
(1)Without prejudice to paragraph
(3), in cases where an individual dose measurement is impossible or inadequate either because

loss or damage to a dose meter or for any other reason, the undertaking shall in the case

a Category A worker - (a) estimate the dose to the exposed worker either from individual measurements made on other exposed workers or from the results

surveillance

the workplace as provided for in Article 21, (b) notify the worker

the dose estimated in accordance with subparagraph (a), (

  1. c)arrange for the approved dosimetric service or the approved radon measurement laboratory, as appropriate, to enter the dose in the individual's dose record and to identify it as an estimated dose, (
  2. d)in cases

accidental or emergency exposure, inform the Institute in writing

the estimated dose, including the methodology applied.

(2)The undertaking shall ensure that the data used in calculating the estimated dose are retained for a period

at least 5 years from the date on which they were recorded.

(3)Where there is reason to believe that the dose received by an exposed worker is much greater or less than that recorded on the dose meter, the undertaking shall also comply with the requirements specified in paragraph
(1).
(4)Where the Institute considers that any estimation made in accordance with paragraph
(1)is inadequate, it may direct the undertaking to carry out whatever additional investigations the Institute considers necessary in order to establish the estimated dose, and the undertaking shall comply with that direction.
(5)Where the Institute is notified

an estimated dose under paragraph

(1)(d), the subsequent entry in the individual's dose record shall be subject to the approval

the Institute. Approval

Dosimetric Services and Radon Measurement Laboratories. 24.

(1)A dosimetric service or a radon measurement laboratory shall not do any act in pursuance

this Order unless - (a) in a case where its principal place

business is in the State, it complies with the general criteria for the operation

testing laboratories specified in European Standard EN 45001 (or its equivalent for the time being) and is accredited for the purposes

this Order by the National Accreditation Board or such other body as the Minister may appoint for the purposes

this Article, and (b) in a case where its principal place

business is in a Member State (other than the State), it is approved by the relevant competent authority for approving or authorising such services or laboratories in that State, or it is accredited by a body that is recognised by the European Co-operation for Accreditation as a body which is competent to grant such accreditation under European Standard EN 45003 (or its equivalent for the time being).

(2)In deciding whether a service or laboratory should be accredited under paragraph
(1)(a), the National Accreditation Board or other body referred to in that paragraph shall - (
  1. a)apply the criteria specified in European Standard EN 45002 (or its equivalent for the time being), and (
  2. b)where appropriate, require the use

proficiency testing schemes.

(3)The National Accreditation Board or other body referred to in paragraph
(1)(a) shall maintain a register

services and laboratories accredited by it under that paragraph.

(4)An approval granted to a dosimetric service or radon measurement laboratory for the purposes

the European Communities (Ionising Radiation) Regulations. 1991 ( S.I. No. 43

1991 ) which is in force immediately before the commencement

this Order shall continue in force in accordance with its terms as if it were an accreditation or approval granted for the purposes

this Order until the date specified in it as the date

expiry or 13 May 2001, whichever date is the earlier. Medical Surveillance

Category A Workers 25.

(1)This Article shall apply to Category A workers and any worker whom an undertaking intends to classify as a Category A worker.
(2)Without prejudice to the duties

the undertaking under this Order, the undertaking shall appoint a registered medical practitioner to carry out medical surveillance

each worker to whom this Article applies who is employed or retained by it (and a registered medical practitioner who is so appointed is referred to in this Order as an “approved medical practitioner”).

(3)The medical surveillance referred to in paragraph
(2)shall be based on the principles that govern occupational medicine and must allow for ascertaining the state

health

workers under surveillance as regards their fitness for the tasks assigned to them.

(4)The undertaking shall provide the approved medical practitioner with access to any relevant information and records that he or she may require including information and records with regard to the environmental conditions existing in the working premises.
(5)The medical surveillance referred to in paragraphs
(2)and
(3)shall include - (a) a medical examination

the worker prior to his or her being classified as a Category A worker; the purpose

this examination shall be to determine the worker's fitness for a post as a Category A worker for which he or she is being considered, and (b) periodic reviews

his or her health.

(6)The review referred to in paragraph
(5)(b) shall be conducted at least once a year or at such lesser intervals as the approved medical practitioner considers necessary and shall be conducted for the purpose

determining whether or not the worker is fit to perform his or her duties. The nature

such a review shall depend on the type

work and on the individual's state

health

(7)If the approved medical practitioner indicates the need for such surveillance the undertaking shall arrange for the medical surveillance under this Article by such a practitioner to be continued for such period after the worker concerned has ceased to be employed or retained by the undertaking as the approved medical practitioner specifies.
(8)The approved medical practitioner shall adopt the following medical classification with respect to fitness for work as a Category A Worker - (a) fit. (b) fit. subject to certain conditions. or (c) unfit.
(9)The undertaking shall ensure that no worker is employed or classified for any period in a particular post as a Category A worker if the medical findings

the approved medical practitioner deem him or her unfit for that post.

(10)If the approved medical practitioner has determined that a worker is fit for work subject to certain conditions, the undertaking shall not employ or retain or continue to employ or retain the worker as a Category A worker unless it complies with those conditions.
(11)The undertaking shall ensure that a health record, containing the particulars specified in Schedule 3, is made and kept up to date for each worker to whom this Article applies and that it is retained until - (i) the worker has or would have attained 75 years

age, or (ii) the expiry

the period

50 years from the date on which that worker has ceased to do the work involving exposure, whichever is the later. Special Medical Surveillance

Exposed Workers 26.

(1)The undertaking shall provide such medical surveillance in addition to that required by Article 25 as is appropriate in each case where a worker, apprentice or student has received an exposure in excess

the dose limits specified in Schedule 2.

(2)In the case

workers referred to in paragraph

(1), the undertaking shall ensure that any determination by it with regard to the subsequent conditions for the exposure

these persons is approved

by the approved medical practitioner.

(3)In addition to the medical surveillance

exposed workers provided for in this Order, the undertaking shall make provision for any further actions in relation to the health protection

the exposed individual considered necessary by the approved medical practitioner, such as further examinations, decontamination measures or urgent remedial treatment.

(4)Any person aggrieved by - (a) a decision made by the approved medical practitioner under Article 25
(8)with respect to fitness for work, (b) a decision made by the undertaking as to the extent

medical surveillance to be provided under paragraph

(1), or (c) a determination made by the undertaking under paragraph
(2), may appeal to the High Court against that decision or determination.
(5)The High Court, on the hearing

an appeal under paragraph

(4), may, as it thinks appropriate, affirm the decision or determination concerned or modify it in such manner as it thinks fit. Operational Protection

Apprentices, Students and Outside Workers 27.

(1)The exposure conditions and operational protection provided by the undertaking for apprentices and students aged 18 years or more shall be equivalent to that

exposed workers

Category A or B, as appropriate.

(2)The exposure conditions and operational protection provided by the undertaking for apprentices and students aged 16 years or more but less than 18 years shall be equivalent to that

exposed workers

Category B.

(3)The undertaking shall ensure, in relation to the exposure

outside workers, that the provisions

Articles 8, 9, 10, 11 and 12 are applied to outside workers. Control

Radioactive Substances, Nuclear Devices and Irradiating Apparatus 28.

(1)This Article applies to practices only.
(2)The undertaking shall - (a) maintain an up to date inventory

the locations and quantities

radioactive substances, irradiating apparatus and other nuclear devices to which the licence granted to it in accordance with Article 4 applies. (b) if it has in its possession, handles or deals with unsealed radioactive substances. maintain records

the quantities

all unsealed radioactive substances used by it and

the dates and method

disposal, (

  1. c)ensure that the inventory referred to in subparagraph (
  2. a)and the records referred to in subparagraph (
  3. b)are readily available for inspection at all reasonable times by the Institute. (
  4. d)when required by the Institute, provide to the Institute copies

the inventory referred to in subparagraph (

  1. a)and the records referred to in subparagraph (b), and (
  2. e)retain the inventory referred to in subparagraph (
  3. a)for at least 2 years from the date

disposal

the items listed in it or, if those items are disposed

on different dates, the last date on which such an item is disposed

(3)The undertaking shall ensure that - (
  1. a)radioactive substances, nuclear devices and irradiating apparatus are clearly labelled as such at all times, and (
  2. b)when not in use, radioactive substances are segregated from non-radioactive substances and kept in secure and safe storage.
(4)The undertaking shall take whatever steps are appropriate to prevent leakage

any radioactive substance from its container or other measures for that protection as far as is practicable.

(5)The undertaking shall ensure, in the case

radioactive substances, that - (a) suitable tests are carried out to detect leakage

any radioactive substance from its container at least once every 2 years or more frequently if recommended by the manufacturer or supplier or if the Institute directs it to do so, (b) in the case

suspected damage to any container or other protection, a leakage test is undertaken immediately; if the removed activity is in excess

200 Bq. use

the radioactive substance shall be discontinued forthwith, and (c) a suitable record

every test is made and retained until such time as the radioactive substance involved has been disposed

or a further record is made in respect

that radioactive substance and that such records are available for inspection by the Institute. Duties

Exposed and Outside Workers, Apprentices, Students and Outside Undertakings 29.

(1)An exposed worker, outside worker, apprentice or student shall - (a) not knowingly expose himself or herself or any other person to ionising radiation to an extent greater than is reasonably necessary for the purpose

his or her work, and shall exercise reasonable care while carrying out such work, (b) make full and proper use

any personal protective equipment provided, (

  1. c)forthwith report to the undertaking any defect he or she discovers in any such equipment, and (
  2. d)notify the undertaking

any suspected exposure likely to cause a breach

any dose limit specified in Schedule 2 or any other unusual occurrence causing or likely to cause exposure in excess

such a limit.

(2)(
  1. a)An outside undertaking shall ensure that each outside worker employed by it is provided with an individual radiation passbook which shall be non-transferable and in which there shall be entered the particulars specified in Schedule 4. (
  2. b)A self-employed outside worker shall furnish himself or herself with a radiation passbook which shall be non-transferable and in which there shall be entered the particulars specified in Schedule 4. (
  3. c)An outside undertaking or a self-employed outside worker shall make suitable arrangements to ensure that the particulars entered in the radiation passbook concerned are kept up to date. (
  4. d)A reference in this Article to a radiation passbook is a reference to such a book that is made available to the outside undertaking or self-employed outside worker concerned by the Institute on request being made

it in that behalf.

(3)An outside worker shall - (a) take reasonable care

the radiation passbook provided or made available to him or her, and, in case he or she is an employed outside worker, if it is lost, report the loss forthwith to the outside undertaking, (b) not misuse the radiation passbook provided or made available to him or her or falsify or attempt to falsify any

the information contained in it, (

  1. c)in case he or she is an employed outside worker, return the radiation passbook to the outside undertaking immediately on ceasing to be employed or retained by that undertaking or when the radiation passbook is full and requires renewal, and (
  2. d)make the radiation passbook available to the undertaking on whose premises he or she carries out services.

(4)Where an outside worker who has lost a passbook subsequently finds it, he or she shall, in case he or she is an employed outside worker, forthwith report its finding to the outside undertaking concerned and return that passbook to the undertaking. Part 6 WORK ACTIVITIES INVOLVING NATURAL RADIATION SOURCES Identification

Work Activities Involving Significant Exposure to Radon 30.

(1)To determine if a workplace is one to which this Order applies by virtue

Article 3

(2)(a), an employer or self employed person who is responsible for a workplace falling within subparagraph (a), (b) or (c)

paragraph

(2)shall measure the radon concentrations in that workplace on being directed to do so by the Institute.
(2)The workplaces referred to in paragraph
(1)are - (
  1. a)all underground workplaces, including mines and show caves, (
  2. b)above ground workplaces in High Radon Areas, (
  3. c)other workplaces which may be identified by the Institute as being liable to have radon concentrations in excess

400 Bq m3, averaged over a minimum period

3 months.

(3)The radon measurements referred to in paragraph
(1)shall be carried out - (
  1. a)by an approved radon measurement laboratory, and (
  2. b)in accordance with the criteria specified in the direction concerned given by the Institute under paragraph
(1).
(4)The results

the radon measurements referred to in paragraph

(1)shall be submitted to the Institute within 6 months from the date

the direction concerned being given to the employer or self-employed person or within such other period as the Institute may specify in the direction. Remedial Measures 31.

(1)If the result

any

the radon measurements referred to in Article 30

(1)exceeds 400 B qm-3 averaged over a minimum period

3 months, the undertaking shall evaluate whether remedial measures to reduce the radon concentration should be taken having regard to such guidelines as may be issued by the Institute for the purposes

the Order in this regard.

(2)If the evaluation referred to in paragraph
(1)shows that the taking

remedial measures is justified, the undertaking shall take the measures as soon as practicable.

(3)Following the taking

remedial measures pursuant to paragraph

(2), the undertaking shall carry out further radon measurements to determine whether the radon concentration in the workplace has been reduced below 400 Bq m-3, averaged over a minimum period

3 months.

(4)The undertaking shall submit to the Institute particulars

any remedial measures taken pursuant to paragraph

(2)and the result

the radon measurements referred to in paragraph

(3). Identification

Work Activities Involving Significant Exposure to Natural Radiation Sources Other Than Radon 32.

(1)To determine if a workplace is one to which this Order applies by virtue

Article 3

(2)(b), an employer or self-employed person who is responsible for a workplace where elevated levels

naturally occurring radionuclides may be present, such as in the oil and gas industries, metal smelting or in sectors involving the manufacture or use

thoriated products, shall investigate the extent

any exposure

workers or members

the public on being directed to do so by the Institute.

(2)The investigation referred to in paragraph
(1)shall be carried out in accordance with methods specified in the direction concerned given by the Institute.
(3)The result

the investigation referred to in paragraph

(1)shall be submitted to the Institute within 6 months from the date

the direction concerned being given to the employer or self-employed person or within such other period as the Institute may specify in the direction. Protection

Air Crew against exposure to cosmic radiation 33.

(1)Each air operator and each undertaking in the State which operates an aircraft shall evaluate the extent

the exposure

air crew from cosmic radiation in accordance with such guidelines as may be issued by the Institute for the purposes

the Order in this regard.

(2)The air operator or undertaking referred to in paragraph
(1)shall submit a written report in relation to the evaluation referred to in that paragraph to the Institute within - (a) in case it holds an air operator's certificate which was in force immediately before the commencement

this Order, 1 year from that commencement. (b) in case it holds an air operator's certificate which was granted on or after the commencement

this Order, 3 months from the making

the evaluation.

(3)If the result

the evaluation referred to in paragraph

(1)shows that air crew are liable to be subject to exposure to cosmic radiation in excess

1 mSv in a period

12 months, the air operator or undertaking referred to in paragraph

(1)shall - (a) assess the exposures

that air crew by methods that have been approved

by the Institute prior to the assessment being carried out, (

  1. b)keep records relating to the assessment referred to in subparagraph (
  2. a)in a manner specified by the Institute, (
  3. c)at the request

any member

the air crew concerned make available to that member a copy

any dose record kept for the purposes

subparagraph (

  1. b)in relation to that member, (
  2. d)provide the Institute with summaries

all such current dose records relating to that year within 3 months

the end

each calendar year, (e) inform that air crew

the health risks involved in their work.

(4)An air operator or an undertaking referred to in paragraph
(1)shall organise the working schedules

air crew liable to receive an exposure to cosmic radiation in excess

6 mSv in a period

12 months with a view to reducing their exposures.

(5)An air operator or an undertaking referred to in paragraph
(1)whereby female air crew are liable to receive an exposure to cosmic radiation in excess

1mSv in a period

12 months shall apply the provisions

Article 11

relating to the obligations

an undertaking. Part 7 RADIATION PROTECTION

THE POPULATION FOR PRACTICES IN NORMAL CIRCUMSTANCES Protection

the Public 34.

(1)An undertaking shall take such measures as are necessary to ensure the best possible protection

the population having regard to the provisions

Articles 8, 9 and 10 and the fundamental principles governing operational protection

the population.

(2)The undertaking shall provide a statement in writing to the Institute upon being requested to do so by it,

the measures it is taking for that purpose.

(3)For the purposes

this Order, “operational protection

the population” means, in normal circumstances, all arrangements and surveys for detecting and eliminating the factors which, in the course

any operation involving exposure to ionising radiation, are liable to create a risk

exposure to members

the public in excess

1 mSv in a period

12 months.

(4)Where relevant to a practice, the Institute shall, before granting a licence in respect

the practice or amending any condition attached to such a licence and as a condition for doing either

those things - (a) require the undertaking to submit to the Institute for examination and approval, from the point

view

radiation protection, plans for installations involving an exposure risk and for the proposed siting

such installations, (

  1. b)require the undertaking not to accept into service any additional or replacement installations unless the Institute has been satisfied that adequate protection has been provided against any exposure or radioactive contamination liable to extend beyond the site perimeter, taking into account, if relevant, demographic, meteorological, geological, hydrological and ecological conditions, and (
  2. c)require the undertaking to submit to the Institute for examination and approval plans for the discharge

radioactive effluents.

(5)The undertaking shall ensure that a practice in respect

which a licence has been granted is carried on in accordance with the principles

health protection

the population as they relate to radiation protection and in particular shall do the following things within its installation - (a) achieve and maintain an optimal level

protection

the environment and the population, (b) check the effectiveness

technical devices for protecting the environment and the population, (c) operate such equipment and follow such procedures as are necessary for measuring and assessing, as appropriate, exposure and radioactive contamination

the environment and the population, and (d) undertake regular calibration

measuring instruments and regular checking that they are serviceable and being correctly used.

(6)The undertaking shall ensure that, in discharging its obligations under paragraphs
(1),
(3),
(4)and
(5), it receives the advice and support

the radiation protection adviser. Estimates

Population Doses 35.

(1)(a) The Institute shall make estimates from time to time

the dose received by the population from practices in relation to which licences have been granted. (b) Whenever and so

ten as the Institute gives a direction to it in that behalf, the undertaking shall make realistic as possible estimates

the doses received by the population as a result

any practice carried on by it. Such estimates shall include estimates

the doses to reference groups in all places where such groups may occur.

(2)The dose estimates referred to in paragraph
(1)(
  1. b)shall, taking into account the radiological risks, include - (
  2. a)assessment

the doses due to external radiation indicating, where appropriate, the quality

the radiation in question, (b) assessment

the intake

radionuclides indicating the nature

the radionuclides and, where necessary, their physical and chemical status and the determination

the activity and concentrations

those radionuclides, (c) assessment

the doses that the reference groups

the population are liable to receive and specification

the characteristics

those groups.

(3)The undertaking shall submit the estimates referred to in paragraph
(1)(b) to the Institute to enable it to make estimates

the dose referred to in paragraph

(1)(a).
(4)The Institute shall keep records relating to the dose estimates referred to in paragraph
(1)(b) including measurements

external exposure, estimates

radioactive intakes and contamination as well as the results

assessments

doses received by reference groups and by the population. Part 8 INTERVENTION AND EMERGENCY PREPAREDNESS Intervention Principles 36.

(1)This Article applies to interventions in cases

radiological emergencies or in cases

lasting exposure resulting from the after effects

a radiological emergency or a past or old work practice or work activity.

(2)The implementation and extent

any intervention shall be considered in conformity with the following principles - (a) intervention shall be undertaken only if the reduction in detriment due to radiation is sufficient to justify the harm and costs, including social costs,

the intervention, (b) the form, scale and duration

the intervention shall be optimised so that the benefits

the reduction in health detriment less the detriment associated with the intervention, will be maximised, (

  1. c)dose limits specified in Schedule 2 shall not apply to intervention, (
  2. d)such intervention levels as are determined by the Institute from time to time shall be regarded as indications as to the situations in which intervention is appropriate, and (
  3. e)in cases

long term exposure to which Article 40 applies, the dose limits specified in Schedule 2 should normally be appropriate for workers involved in interventions.

(3)Where the intervention is necessary in respect

a particular radiological emergency, the undertaking shall comply with the provisions

subparagraphs (b) to (e)

paragraph

(2)after consultation with the Institute on the intervention measures considered appropriate and in accordance with any guidance given to it by the Institute in relation to that matter. Intervention Preparation and Plans 37.
(1)This Article applies to emergencies arising from events taking place either inside or outside the country.
(2)In the case

a practice in relation to which a licence has been granted, the undertaking carrying on the practice shall, when directed in writing by the Institute to do so - (a) evaluate the possibility

a radiological emergency resulting from the practice which would give rise to significant hazards to members

the public, (b) evaluate the likely spatial and temporal distribution

the radioactive substances dispersed in the event

such an emergency and the corresponding potential exposures, (

  1. c)prepare an appropriate intervention plan to deal with such an emergency: that intervention plan shall be prepared after consultation with the Institute and the local authority within whose functional area the undertaking carries on the practice, hereafter in this Order referred to as “the relevant local authority”, (
  2. d)submit a copy

the intervention plan referred to in subparagraph (

  1. c)to the Institute and the relevant local authority as soon as may be after it is prepared, (
  2. e)carry out drills and exercises to test the intervention plan at regular intervals, (
  3. f)ensure that, where appropriate, suitably trained personnel are available for technical, medical and health intervention, and (
  4. g)ensure that any person under the control

the undertaking who may be involved in or may be affected by the intervention plan is given suitable instruction in the arrangements

the plan.

(3)After consultation with any other Minister

the Government who might, in the opinion

the Minister, be concerned in the matter, the Minister shall prepare a plan which shall be known as the “National Emergency Plan for Nuclear Accidents” and is in this Article referred to as “the plan”.

(4)The plan shall make provision for radiological emergencies that might occur in connection with practices taking place both inside and outside the country and shall include the following - (a) provision for the issue and receipt

notifications and other information about radiological emergencies that may occur, (b) the organisation

appropriate intervention, taking account

the characteristics

the radiological emergency, (c) the assessment and recording

the consequences

the radiological emergency and

the effectiveness

the intervention, (d) specifying the duties

Ministers

the Government, local authorities and other public bodies with regard to the measures to be taken under the plan and the procedures to be followed by them for the purposes

co-ordinating those measures, (e) the procedures for the assessment

technical information related to any emergency or potential emergency, (f) the criteria for evaluating the need for intervention and, if appropriate, procedures for the implementation

countermeasures, and (g) the procedures for ensuring that the public is kept fully informed

the nature and extent

any risks to which they might be exposed and

any actions taken to minimise or reduce such risks.

(5)The Minister, after consultation with the Institute, shall arrange for the carrying out

drills and exercises to test the plan at suitable intervals and may amend the plan from time to time. Dealing with Radiological Emergencies 38.

(1)An undertaking carrying on a practice shall, immediately upon a radiological emergency arising from the practice, notify the Institute

the emergency. At the same time the undertaking shall inform the local emergency services

the circumstances with respect to the emergency.

(2)In relation to such an emergency, the undertaking shall make an initial provisional assessment

the circumstances surrounding, and the possible consequences

, the emergency and submit a statement in writing

that assessment to the Institute as soon as possible but not later than 24 hours after the commencement

the emergency.

(3)The undertaking shall undertake or assist with any intervention appropriate to the circumstances

the radiological emergency.

(4)The intervention referred to in paragraph
(3)shall include, if the situation so requires, intervention related to - (a) the source, to reduce or stop the direct radiation and emission

radionuclides, (b) the environment, to reduce the transfer

radioactive substances to individuals, and (c) individuals, to reduce exposure and organise the treatment

victims.

(5)The person taking the intervention measures under this Article and the local authority or authorities, in whose functional area or areas these measures are being taken, shall co-operate with one another with regard to those measures.
(6)Any plans prepared by local authorities to deal with major emergencies shall include provision for the organisation

the intervention measures which may be required to be taken within their functional areas in the event

a radiological emergency occurring. Emergency Occupational Exposure 39.

(1)The Institute shall prepare and publish guidelines with regard to the maximum level

doses, in excess

those specified in Schedule 2. workers or other persons involved in taking intervention measures ought to be exposed to in taking such measures.

(2)In preparing such guidelines, the Institute shall take account

the technical obligations and health risks associated with the intervention concerned.

(3)An exposure

a worker or other person referred to in paragraph

(1)to a dose in excess

the limits indicated in the guidelines prepared under that paragraph may be permitted to save human lives but only if he or she volunteers for such exposure having been fully informed about the risks concerned.

(4)Any person responsible for the organisation

intervention measures shall provide radiological monitoring and medical surveillance for those involved in the taking

the measures. Intervention in Cases

Lasting Exposure 40.

(1)This Article applies to situations leading to lasting exposure resulting from the after-effects

a radiological emergency or a practice which has ceased to be carried on.

(2)Where the lasting exposure is the result

a practice, the undertaking which carries on or, as the case may be, carried on the practice shall, to the extent that it may be necessary, ensure that - (a) the area concerned is demarcated, (b) arrangements for the monitoring

exposure are made, (c) any appropriate intervention is implemented, taking account

the real characteristics

the situation, and (d) access to or use

land or buildings situated in the demarcated area is regulated.

(3)The undertaking concerned, the Institute and the local authority or authorities in whose functional area or areas the measures and arrangements referred to in paragraph
(2)are being taken or made shall co-operate with one another with regard to those measures and arrangements. Part 9 NOTIFICATIONS, NOTICES AND REVOCATION Notifications 41.
(1)The undertaking shall notify, in each year, the relevant fire

ficer

the location. nature and amount

all radioactive substances held by it for the time being.

(2)In paragraph
(1)“relevant fire

ficer” means the person designated to receive such a notification by the fire authority (within the meaning

the Fire Services Act, 1981 (No. 30

1981)), in whose functional area the practice or work activity concerned is carried on.

(3)If any, loss, larceny or other misappropriation

any radioactive substance, nuclear device or irradiating apparatus held by it occurs, the undertaking shall, immediately after the loss, larceny or misappropriation takes place, notify the Institute

the loss, larceny or misappropriation.

(4)Where an undertaking suspects or has been informed that an occurrence referred to in paragraph
(3)has or may have taken place, it shall immediately make an investigation

the matter and submit a report

the investigation to the Institute as soon as possible.

(5)If - (
  1. a)a radioactive substance under the undertaking's control has been released or is likely to have been released into the atmosphere as a gas, aerosol or dust or has been spilled or otherwise released in such manner as to give rise to significant contamination, and (
  2. b)the quantity

radioactive substance involved exceeds 10 times the quantity specified for that substance in Annex I and 100 times the concentration figure specified for that substance in Annex I, then the undertaking shall, immediately after the release or spillage takes place, notify the Institute

the release or spillage. Enforcement Notices 42.

(1)If an inspector is

the opinion that an undertaking or an air operator has contravened or is contravening a provision

this Order, the inspector may serve on the undertaking or air operator a notice in writing (in this Order referred to as “an enforcement notice”) requiring it to do or not to do such things as are specified in the notice for the purpose

ensuring compliance with the provision concerned.

(2)Without prejudice to paragraph
(1), an enforcement notice may require the undertaking or air operator concerned to either or both - (a) cease the carrying on

the practice or work activity concerned, (b) mitigate or remedy any effects

the contravention concerned.

(3)An enforcement notice shall take effect - (
  1. a)if the notice so provides, immediately upon its being received by the undertaking or air operator concerned (but without prejudice to paragraph 7), (
  2. b)in any other case - (
  3. i)if no appeal under this Article is made against the notice, on the expiration

the period referred to in paragraph

(4)or the day specified in the notice on which it is to take effect, whichever is the later, or (ii) if such an appeal is made - (I) on the day next following the day on which the appeal is confirmed under paragraph
(5)or withdrawn. or (II) on the day specified in the notice on which it is to take effect, whichever is the later.
(4)An undertaking or air operator on which an enforcement notice is served may, within the period

14 days beginning on the day on which the notice is served on it, appeal to the appropriate judge

the District Court against the notice.

(5)On the hearing

an appeal under paragraph

(4)the court may, as it thinks proper, (
  1. a)confirm the notice unconditionally, (
  2. b)make such modifications to the notice as it considers appropriate and confirm this notice, as so modified, or (
  3. c)cancel the notice.
(6)Notwithstanding that it has been confirmed under paragraph
(5), the appropriate judge

the District Court may, on the hearing

the appeal under paragraph

(4)in relation to it, if the undertaking or air operator concerned make an application to him or her in that behalf, suspend the operation

an enforcement notice for such period as in the circumstances

the case he or she considers appropriate.

(7)The making

an appeal under paragraph

(4)shall not have the effect

suspending the operation

the enforcement notice concerned but the undertaking or air operator concerned may apply to the appropriate judge

the District Court for an order suspending the operation

the notice until the conclusion

the appeal and the court may, on the hearing

such an application, grant or refuse to grant such an order.

(8)An inspector may cancel an enforcement notice served under this Article (other than such a notice that has been confirmed under paragraph
(5)).
(9)An inspector may apply to the appropriate judge

the District Court for an order cancelling an enforcement notice that has been confirmed under paragraph

(5)and the court shall, on the hearing

the application, unless it sees good reason to the contrary, grant such an order.

(10)In this Article “appropriate judge

the District Court” means the judge

the District Court for the District Court district in which the enforcement order concerned was served. Revocation 43.

(1)The Radiological Protection Act, 1991 (General Control

Radioactive Substances, Nuclear Devices and Irradiating Apparatus) Order, 1993 ( S.I. No 151

1993 ), is hereby revoked. SCHEDULE 1 INFORMATION TO BE PROVIDED IN A LICENCE APPLICATION FOR A PRACTICE OR NOTIFICATION

A WORK ACTIVITY Article 6

(2)1. The name and address

the undertaking and a telephone number, fax number or electronic mail address at which it can be contacted at that address. 2. The address

the premises where or from where the practice or work activity is to be carried on and a telephone number, fax number or electronic mail address at which the undertaking can be contacted at that address. 3. The nature and business

the undertaking. 4. Into which

the following categories the source or sources

ionising radiation concerned fall - (

  1. a)nuclear device/sealed source, (
  2. b)unsealed radioactive substance, (
  3. c)irradiating apparatus, (
  4. d)an atmosphere containing short-lived daughters

radon, (e) cosmic radiation. 5. In the case

subparagraphs (a), (b) and (c)

paragraph 4, the addresses

any premises, other than the address stated under paragraph 2, at which the source or each source

ionising radiation is to be used. 6. In the case

an application for a licence in respect

a practice, the proposed date

commencement

the practice. 7. In the case

a work activity, the date

commencement

the work activity. 8. In the case

an application for a licence in respect

a practice, the following additional information if the Institute requires it: (a) a description

the work with ionising radiation, (b) particulars

the sources

ionising radiation, (c) the quantities

any radioactive substances involved, (d) the identity

any person engaged in the practice, and (e) the name

the radiation protection adviser. SCHEDULE 2 DOSE LIMITS FOR EXPOSED WORKERS, APPRENTICES, STUDENTS AND MEMBERS

THE PUBLIC Article 10

(1)Dose Limits for Exposed Workers 1.
(1)The limit on effective dose for an exposed worker shall be 20 mSv in a period

12 months.

(2)Without prejudice to subparagraph
(1)- (a) the limit on equivalent dose for the lens

the eye

such a worker shall be 150 mSv in a period

12 months, (b) the limit on equivalent dose for the skin

such a worker shall be 500 mSv in a period

12 months; this limit shall apply to the dose averaged over any area

1 cm2, regardless

the area exposed, (c) the limit on equivalent dose for the hands, forearms, feet and ankles

such a worker shall be 500 mSv in a period

12 months.

(3)Notwithstanding subparagraphs
(1)and
(2), as soon as a pregnant exposed worker informs the undertaking

her condition, the equivalent dose to the child to be born shall be limited to 1 mSv for the remainder

the pregnancy. Dose Limits for Apprentices and Students 2.

(1)The dose limits for an apprentice or student aged 18 years or over who, in the course

his or her studies, is obliged to use sources shall be the same as the dose limits for an exposed worker specified in paragraph 1

this Schedule.

(2)The limit

effective dose for an apprentice or student aged 16 years or more but less than 18 years who, in the course

his or her studies, is obliged to use sources shall be 6 mSv in a period

12 months.

(3)Without prejudice to subparagraph
(2)- (a) the limit on equivalent dose for the lens

the eye

an apprentice or student referred to in that subparagraph shall be 50 mSv in a period

12 months. (b) the limit on equivalent dose for the skin

such an apprentice or student shall be 150 mSv in a period

12 months; this limit shall apply to the dose averaged over any area

1 cm2 regardless

the area exposed, (c) the limit on equivalent dose for the hands, forearms, feet and ankles

such an apprentice or student shall be 150 mSv in a period

12 months.

(4)The dose limits for an apprentice or student to whom subparagraphs
(1)and
(2)do not apply shall be the same as the dose limits for members

the public specified in paragraph 3. Dose Limits for Members

the Public 3.

(1)The limit on effective dose for a member

the public shall be 1 mSv in a period

12 months.

(2)Without prejudice to subparagraph
(1)- (a) the limit on equivalent dose for the lens

the eye shall be 15 mSv in a period

12 months. (b) the limit on equivalent dose for the skin shall be 50 mSv in a period

12 months averaged over any 1 cm2

skin, regardless

the area exposed. SCHEDULE 3 INFORMATION TO BE CONTAINED IN A HEALTH RECORD Article 25

(11)1. The worker's full name, gender, date

birth, permanent address and RSI number. 2. The date

the worker's commencement as a Category A worker in his or her present employment. 3. The date

the last medical examination or health review carried out under this Order in respect

the worker. 4. The results

that last such examination or review. 5. The comments (if any)

the approved medical practitioner as to the worker's fitness to work or as to the conditions to which the worker should be subject. 6. The signature

the approved medical practitioner. SCHEDULE 4 PARTICULARS TO BE CONTAINED IN A RADIATION PASSBOOK Article 22

(8)(a)
  1. Individual serial number.
  2. A statement that the passbook has been issued by the Institute.
  3. Date

issue

the passbook. 4. Name and address

the outside undertaking. 5. Full name, date

birth, gender and RSI number

the outside worker who will hold the passbook. 6. Date

the last medical review

the outside worker and his or her classification as fit. fit subject to conditions (which shall be specified) or unfit. 7. In respect

each assignment carried out by the outside worker, the following particulars - (a) name

the undertaking where the services are carried out, (

  1. b)period covered by the assignment, (
  2. c)latest available cumulative annual dose assessment, (
  3. d)an estimate

the effective dose received by the outside worker, (e) in the event

a non-uniform exposure, an estimate

the dose equivalent in the different parts

the body, (f) in the event

an internal contamination, an estimate

the effective dose. SCHEDULE 5 TEXT

ANNEX I

COUNCIL DIRECTIVE 96/29/EURATOM CRITERIA TO BE CONSIDERED FOR THE APPLICATION

ARTICLE 3 1. A practice may be exempted from the requirement to report without further consideration. In compliance with Article 3

(2)(
  1. a)or (
  2. b)respectively, if either the quantity or the activity concentration, as appropriate,

the relevant radionuclides does not exceed the values in column 2 or 3

Table A. 2. The basic criteria for the calculation

the values in Table A, for the application

exemption for practices, are as follows: (a) the radiological risks to individuals caused by the exempted practice are sufficiently low as to be

no regulatory concern; and (b) the collective radiological impact

the exempted practice is sufficiently low as to be

no regulatory concern under the prevailing circumstances; and (c) the exempted practice is inherently without radiological significance, with no appreciable likelihood

scenarios that could lead to a failure to meet the criteria in (

  1. a)and (b). 3. Exceptionally, as provided in Article 3, individual Member States may decide that a practice may be exempted where appropriate without further consideration, in accordance with the basic criteria, even if the relevant radionuclides deviate from the values in Table A, provided that the following criteria are met in all feasible circumstances: (
  2. a)the effective dose expected to be incurred by any member

the public due to the exempted practice is

the order

10 μSv or less in a year; and (b) either the collective effective dose committed during one year

performance

the practice is no more than about 1 man x Sv or an assessment

the optimization

protection shows that exemption is the optimum option. 4. For radionuclides not listed in Table A, the competent authority shall assign appropriate values for the quantities and concentrations

activity per unit mass where the need arises. Values thus assigned shall be complementary to those in Table A. 5. The values laid down in Table A apply to the total inventory

radioactive substances held by a person or undertaking as part

a specific practice at any point in time. 6. Nuclides carrying the suffix ‘+’ or ‘sec’ in Table A represent parent nuclides in equilibrium with their correspondent daughter nuclides as listed in Table B. In this case the values given in Table A refer to the parent nuclide alone, but already take account

the daughter nuclide(s) present. 7. In all other cases

mixtures

more than one nuclide, the requirement for reporting may be waived if the sum

the ratios for each nuclide

the total amount present divided by the value listed in Table A is less than or equal to 1. This summation rule also applies to activity concentrations where the various nuclides concerned are contained in the same matrix. TABLE A Nuclide Quantity (Bq) Concentration (kBq/kg) H-3 109 106 Be-7 107 103 C-14 107 104 O-15 109 102 F-18 106 10 Na-22 106 10 Na-24 105 10 Si-31 106 103 P-32 105 103 P-33 108 105 S-35 108 105 Cl-36 106 104 Cl-38 105 10 Ar-37 108 106 Ar-41 109 102 K-40 106 102 K-42 106 102 K-43 106 10 Ca-45 107 104 Ca-47 106 10 Sc-46 106 10 Sc-47 106 102 Sc-48 105 10 V-48 105 10 Cr-51 107 103 Mn-51 105 10 Mn-52 105 10 Mn-52m 105 10 Mn-53 109 104 Mn-54 106 10 Mn-56 105 10 Fe-52 106 10 Fe-55 106 104 Fe-59 106 10 Co-55 106 10 Co-56 105 10 Co-57 106 102 Co-58 106 10 Co-58m 107 104 Co-60 105 10 Co-60m 106 103 Co-61 106 102 Co-62m 105 10 Ni-59 108 104 Ni-63 108 105 Ni-65 106 10 Cu-64 106 102 Zn-65 106 10 Zn-69 106 104 Zn-69m 106 102 Ga-72 105 10 Ge-71 108 104 As-73 107 103 As-74 106 10 As-76 105 102 As-77 106 103 Se-75 106 102 Br-82 106 10 Kr-74 109 102 Kr-76 109 102 Kr-77 109 102 Kr-79 105 103 Kr-81 107 104 Kr-83m 1012 105 Kr-85 104 105 Kr-85m 1010 103 Kr-87 109 102 Kr-88 109 102 Rb-86 105 102 Sr-85 106 102 Sr-85m 107 102 Sr-87m 106 102 Sr-89 106 103 Sr-90+ 104 102 Sr-91 105 10 Sr-92 106 10 Y-90 105 103 Y-91 106 103 Y-91m 106 102 Y-92 105 102 Y-93 105 102 Zr-93 + 107 103 Zr-95 106 10 Zr-97 + 105 10 Nb-93m 107 104 Nb-94 106 10 Nb-95 106 10 Nb-97 106 10 Nb-98 105 10 Mo-90 106 10 Mo-93 108 103 Mo-99 106 102 Mo-101 106 10 Tc-96 106 10 Tc-96m 107 103 Tc-97 108 103 Tc-97m 107 103 Tc-99 107 104 Tc-99m 107 102 Ru-97 107 102 Ru-103 106 102 Ru-105 106 10 Ru-106 + 105 102 Rh-103m 108 104 Rh-105 107 102 Pd-103 108 103 Pd-109 106 103 Ag-105 106 102 Ag-108m + 106 10 Ag-110m 106 10 Ag-111 106 103 Cd-109 106 104 Cd-115 106 102 Cd-115m 106 103 In-111 106 102 In-113m 106 102 In-114m 106 102 In-115m 106 102 Sn-113 107 103 Sn-125 105 102 Sb-122 104 102 Sb-124 106 10 Sb-125 106 102 Te-123m 107 102 Te-125m 107 103 Te-127 106 103 Te-127m 107 103 Te-129 106 102 Te-129m 106 103 Te-131 105 102 Te-131m 106 10 Te-132 107 102 Te-133 105 10 Te-133m 105 10 Te-134 106 10 I-123 107 102 I-125 106 103 I-126 106 102 I-129 105 102 I-130 106 10 I-131 106 102 I-132 105 10 I-133 106 10 I-134 105 10 I-135 106 10 Xe-131m 104 104 Xe-133 104 103 Xe-135 1010 103 Cs-129 105 102 Cs-131 106 103 Cs-132 105 10 Cs-134m 105 103 Cs-134 104 10 Cs-135 107 104 Cs-136 105 10 Cs-137+ 104 10 Cs-138 104 10 Ba-131 106 102 Ba-140 + 105 10 La-140 105 10 Ce-139 106 102 Ce-141 107 102 Ce-143 106 102 Ce-144 + 105 102 Pr-142 105 102 Pr-143 106 104 Nd-147 106 102 Nd-149 106 102 Pm-147 107 104 Pm-149 106 103 Sm-151 108 104 Sm-153 106 102 Eu-152 106 10 Eu-152m 106 102 Eu-154 106 10 Eu-155 107 102 Gd-153 107 102 Gd-159 106 103 Tb-160 106 10 Dy-165 106 102 Dy-166 106 103 Ho-166 105 103 Er-169 107 104 Er-171 106 102 Tm-170 106 103 Tm-171 108 104 Yb-175 107 103 Lu-177 107 108 Ta-182 104 10 W-181 107 103 W-185 107 104 W-187 106 102 Re-186 106 103 Re-188 105 102 Os-185 106 10 Os-191 107 102 Os-191m 107 103 Os-193 106 102 Ir-190 106 10 Ir-192 104 10 Ir-194 105 102 Pt-191 106 102 Pt-193m 107 103 Pt-197 106 103 Pt-197m 106 102 Au-198 106 102 Au-199 106 102 Hg-197 107 102 Hg-197m 106 102 Hg-203 105 102 Tl-200 106 10 Tl-201 106 102 Tl-202 106 102 Tl-204 104 104 Pb-203 106 102 Pb-210 + 104 10 Pb-212 + 105 10 Bi-206 105 10 Bi-207 106 10 Bi-210 106 103 Bi-212 + 105 10 Po-203 106 10 Po-205 106 10 Po-207 106 10 Po-210 104 10 At-211 107 103 Rn-220 + 107 104 Rn-222 + 108 10 Ra-223 + 105 102 Ra-224 + 105 10 Ra-225 105 102 Ra-226 + 104 10 Ra-227 106 102 Ra-228 + 105 10 Ac-228 106 10 Th-226 + 107 103 Th-227 104 10 Th-228 + 104 1 Th-229 + 103 1 Th-230 104 1 Th-231 107 103 Th-232sec 103 1 Th-234 + 105 103 Pa-230 106 10 Pa-231 103 1 Pa-233 107 102 U-230 + 105 10 U-231 107 102 U-232 + 103 1 U-233 104 10 U-234 104 10 U-235 + 104 10 U-236 104 10 U-237 106 102 U-238 + 104 10 U-238sec 103 1 U-239 106 102 U-240 107 103 U-240 + 106 10 Np-237 + 103 1 Np-239 107 102 Np-240 106 10 Pu-234 107 102 Pu-235 107 102 Pu-236 104 10 Pu-237 107 103 Pu-238 104 1 Pu-239 104 1 Pu-240 103 1 Pu-241 105 102 Pu-242 104 1 Pu-243 107 103 Pu-244 104 1 Am-241 104 1 Am-242 106 103 Am-242m + 104 1 Am-243 + 103 1 Cm-242 105 102 Cm-243 104 1 Cm-244 104 10 Cm-245 103 1 Cm-246 103 1 Cm-247 104 1 Cm-248 103 1 Bk-249 106 103 Cf-246 106 103 Cf-248 104 10 Cf-250 104 10 Cf-251 103 1 Cf-252 104 10 Cf-253 105 102 Cf-254 103 1 Es-253 105 102 Es-254 104 10 Es-254m 106 102 Fm-254 107 104 Fm-255 106 103 TABLE B List

nuclides in secular equilibrium as referred to in point 6

this Annex Parent nuclide Daughter nuclides Sr-80 + Rb-80 Sr-90 + Y-90 Zr-93 + Nb-93m Zr-97 + Nb-97 Ru-106 + Rh-106 Ag-108m + Ag-108 Cs-137 + Ba-137 Ba-140 + La-140 Ce-134 + La-134 Ce-144 + Pr-144 Pb-210 + Bi-210, Po-210 Pb-212 + Bi-212, Tl-208, Po-212 Bi-212 + Tl-208, Po-212 Rn-220 + Po-216 Rn-222 + Po-218, Pb-214, Bi-214, Po-214 Ra-223 + Rn-219, Po-215, Pb-211, Bi-211, Tl-207 Ra-224 + Rn-220, Po-216, Pb-212, Bi-212, Tl-208, Po-212 Ra-226 + Rn-222, Po-218, Pb-214, Bi-214, Pb-210, Bi-210, Po-210, Po-214 Ra-228 + Ac-228 Th-226 + Ra-222, Rn-218, Po-214 Th-228 + Ra-224, Rn-220, Po-216, Pb-212, Bi-212, Tl-208, Po-212 Th-229 + Ra-225, Ac-225, Fr-221, At-217, Bi-213, Po-213, Pb-209 Th-232sec Ra-228, Ac-228, Th-228, Ra-224, Rn-220, Po-216, Pb-212, Bi-212, Tl-208, Po-212 Th-234 + Pa-234m U-230 + Th-226, Ra-222, Rn-218, Po-214 U-232 + Th-228, Ra-224, Rn-220, Po-216, Pb-212, Bi-212, Tl-208, Po-212 U-235 + Th-231 U-238 + Th-234, Pa-234m U-238sec Th-234, Pa-234m, U-234, Th-230, Ra-226, Rn-222, Po-218, Pb-214, Bi-214, Pb-210, Bi-210, Po-210, Po-214 U-240 + Np-240 Np-237 + Pa-233 Am-242m + Am-242 Am-243 + Np-239 SCHEDULE 6 TEXT

ANNEX II

COUNCIL DIRECTIVE 96/29/EURATOM A. Definitions

terms used in this Annex Ambient dose equivalent H* (d): the dose equivalent at a point in a radiation field that would be produced by the corresponding expanded and aligned field in the ICRU sphere at a depth, d, on the radius opposing the direction

the aligned field. The special name for the unit

ambient dose equivalent is sievert (Sv). Directional dose equivalent H' (d, Ω): the dose equivalent at a point in a radiation field that would be produced by the corresponding expanded field, in the ICRU sphere at a depth, d, on a radius in a specified direction, Ω. The special name for the unit

directional dose equivalent is sievert (Sv). Expanded and aligned field: a radiation field in which the fluence and its directional and energy distribution are the same as in the expanded field, but the fluence is unidirectional. Expanded field: a field derived from the actual field, where the fluence and its directional and energy distributions have the same values throughout the volume

interest as in the actual field at the point

reference. Fluence, Φ: the quotient

dN by da, where dN is the number

particles which enter a sphere

cross-sectional area da: dN Φ = ___ da Mean quality factor DŽ: average value

the quality factor at a point in tissue where the absorbed dose is delivered by particles with different L values. It is calculated according to the expression: where D(L)dL is the absorbed dose at 10 mm between linear energy transfer L and L + dL; and Q(L) is the corresponding quality factor at the point

interest. The Q-L relationships are given in C. Personal dose equivalent, Hp(d): the dose equivalent in soft tissues, at an appropriate depth, d, below a specified point in the body. The special name for the unit

personal dose equivalent is sievert (Sv). Quality factor (Q): a function

linear energy transfer (L) used to weight absorbed does at a point in such a way as to take into account the quality

a radiation. Radiation weighting factor (wR): a dimensionless factor used to weight the tissue or organ absorbed dose. The appropriate (wR) values are given in B. Tissue or organ absorbed dose (DT): the quotient

the total energy impatted in a tissue or organ and the mass

that tissue or organ. Tissue weighting factor (wT): a dimensionless factor used to weight the equivalent dose in a tissue or organ (T). The appropriate (wT) values are specified in D. Unrestricted linear energy transfer (L ∞): a quantity defined as: dE L ∞ = ___ dt where dE is the mean energy lost by a particle

energy E in traversing a distance dl in water. In this Directive L ∞ is denoted by L. ICRU sphere: a body introduced by the International Commission on Radiation Units (ICRU) to approximate the human body as regards energy absorption from ionizing radiation; it consists

a 30 cm diameter tissue equivalent sphere with a density

1 g cm-3 and a mass composition

76.2% oxygen, 11.1% carbon. 10.1% hydrogen and 2.6% nitrogen. B. Values

radiation weighting factor, wR Values

radiation weighting factor, wR, depend on the type and quality

the external radiation field or on the type and quality

the radiation emitted by an internally deposited radionuclide. When the radiation field is composed

types and energies with different values

wR, the absorbed dose must be subdivided into blocks, each with its own value

wR and added to give the total equivalent dose. Alternatively, it may be expressed as a continuous distribution in energy where each element

absorbed dose from the energy element between E and E + dE is multiplied by the value

wR from the relevant entry in the Table below. Type and energy range Radiation weighting factor, wR Photons, all energies 1 Electrons and muons, all energies 1 Neutrons, energy 5 10 keV to 100 keV 10 > 100 keV to 2 MeV 20 > 2 MeV to 20 MeV 10 > 20 MeV 5 Protons, other than recoil protons, energy > 2 MeV 5 Alpha particles, fission fragments, heavy nuclei 20 In calculations involving neutrons, difficulties may arise in applying step function values. In these cases it may be preferable to use the continuous function described by the following mathematical relationship: wR = 5 + 17e-(ln(2E))2/6 where E is the neutron energy in MeV. A direct comparison

the two approaches is given, in Figure 1. Incident neutron energy (MeV) Figure 1 Radiation weighting factors for neutrons. The smooth curve is to be treated as an approximation For radiation types and energy which are not included in the table, an approximation

wR may be obtained by calculating the mean quality factor Q at a depth

10 mm in a ICRU sphere. C. Relationship between the quality factor, Q(L), and unrestricted linear energy transfer, L Unrestricted linear energy transfer, L in water (keV μm-1) Q(L) 1 10-100 0,32L - 2,2 > 100 300/√L D. Values

tissue weighting factor, WT (*) Values

tissue weighting factor, WT, are shown below: Tissue or organ Tissue weighting factors, WT Gonads 0,20 Bone marrow (red) 0,12 Colon 0,12 Lung 0,12 Stomach 0,12 Bladder 0,05 Breast 0,05 Liver 0,05 Oesophagus 0,05 Thyroid 0,05 Skin 0,01 Bone surface 0,01 Remainder 0,05(**) (***) E. Operational quantities for external radiation Operational quantities for external radiation are used for individual monitoring for radiation protection purposes: 1. Individual monitoring: Personal dose equivalent Hp (d), d: depth in mm in the body. 2. Area monitoring: ambient dose equivalent H(*) (d), directional dose equivalent H' (d,Ω), d: depth in mm under the surface

the sphere given in A, Ω: angle

incidence. 3. For strongly penetrating radiation a depth

10 mm, for weakly penetrating radiation a depth

0,07 mm for the skin and 3 mm for the eye is recommended. SCHEDULE 7 TEXT

ANNEX III

COUNCIL DIRECTIVE 96/29/EURATOM A. Throughout the Directive, unless otherwise specified, requirements on doses apply to the sum

the relevant doses from external exposure in a specified perio

🔗 To official source

AI explanation based on the official legal text. Indicative, not a substitute for legal advice.