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Radiation Protection Scheme Workers 2014

Original Language Title: Regeling stralingsbescherming werknemers 2014

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Arrangement of the Minister of Social Affairs and Employment of 21 November 2013, 2013-0000158376 laying down rules implementing the Radiation Protection Decision (Scheme of Radiation Protection Workers 2014)

The Minister for Social Affairs and Employment,

Acting in accordance with the Minister for Economic Affairs;

Having regard to the Articles 7, 2nd and 4 , 7a , 8, second paragraph , 10, fifth paragraph , 20, fourth member , 84, second paragraph , 85, second paragraph , 87, 6th paragraph , 91, second and fifth members , 94, second and fourth members , 111, first paragraph, part b, and fourth paragraph, of the Radiation Protection Decision and Article 19 of the Decision nuclear installations, fissile materials and ores ;

Decision:


§ 1. General

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Article 1. Definitions

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For the purposes of this arrangement:


§ 2. Radiation Doctors

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Article 2. Registration in the Register

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  • 1 The Minister for Economic Affairs shall arrange for a current register in which the radiation doctors are registered.

  • 2 An invitation to tender and renewal shall take place if the applicant:

    • a. As a business doctor, registered in the register of recognized social medicine, which is maintained by the Registration Committee of Medical Specialists of the Royal Netherlands Society for the Promotion of Medicine;

    • (b) holds a diploma relating to training as a coordinating expert, as referred to in Article 3 (1). Article 7f of the Decision -of a diploma relating to training as intended Article 3 of the Temporary Arrangement Recognition of Experts on Radioactive Substances and Equipment 2013 , or subject to compliance with Article 7a of the Decision qualified qualifications; and

    • c. shows that he has maintained the necessary knowledge after obtaining the diploma or qualifications referred to in subparagraph (b), to which requirements are met in any case if the applicant has pursued after-or in-service training; as recorded in Annex A , Section I, to this Arrangement.

  • 3 The invitation to tender shall be for a maximum period of five years. At the end of that period, the invitation to tender may be renewed for a period of not more than five years, provided that the applicant demonstrates that:

    • a. as an occupational doctor is entered in the register of recognized social medicine, maintained by the Registration Committee of Medicinal Products of the Royal Dutch Society for the Promotion of Medicine; and

    • b. has kept the necessary knowledge and experience during the past five-year tendering period, to which requirements are met in any case if the applicant has followed after and by-training activities, as included in Annex A This scheme.

  • 4 The applicant for registration shall give to the Minister for Economic Affairs a certificate of registration as a business doctor and a copy of a diploma or, as far as possible, qualifications referred to in paragraph 2 (b).

  • 5 The Minister for Economic Affairs shall forward the invitation to tender at the request of the registered office or if he reaches any relevant information justifying such cancellation.


§ 3. Dosimetry services and dose registration system

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Article 3. Procedure for recognition of dosimetry services

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  • 1 The Minister for Economic Affairs recognises a dosimetry service at the request of a legal person. He shall ensure publication of the recognition in the Official Gazette and for a current register listing the approved dosimetry services.

  • 2 The application referred to in paragraph 1 shall, in any event, include:

    • a. a general description of the services to be provided;

    • b. The design of the personal dosimetry system applied;

    • c. The dosimetric properties of the dosimeter, including the energy and angular dependence, the detection threshold for different types of radiation and the other performance criteria;

    • d. a description of the method of recording and reporting the measurement data;

    • e. a description of the method of calibration of the readout system and dosimeters, as well as the frequency of calibration;

    • f. a description of the quality assurance and a description of how the data is secured; and

    • g. guarantees for the protection of personal data.

  • 3 A recognition may be refused if the information referred to in the second paragraph is insufficient or incomplete.


Article 4. Regulated dosimetry services

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  • 1 A recognition as intended Article 3 , it shall be granted if:

    • a. the service is entrusted with the management of the personal dosimetry system, including the associated administrative care and the assessment of the readings of the dose meter provided;

    • (b) the service complies with the recommendations of the European Commission, listed in Radiation Protection 73 Technical Recommendations Report EUR 14852 EN (1994);

    • c. the service is accredited according to the criteria, named in NEN-EN-ISO/IEC standard 17025, including the calibration system;

    • d. the daily management and management of the service shall be carried out by a person, who holds a diploma regarding the training to coordinate, intended to Article 7f of the Decision -of a diploma relating to training as intended Article 3 of the Temporary Arrangement Recognition of Experts on Radioactive Substances and Equipment 2013 , or subject to compliance with Article 7a of the Decision the qualifications demonstrated, assisted by a sufficient number of staff appointed for the task and trained for their duties; and

    • e. the service participates in periodic national or international performance studies as specified in ISO 14146 (2000).

  • 2 The approved service provides the Minister and the Minister of Economic Affairs an annual reporting of the information, which is included in Annex B In this arrangement.

  • The Minister for Economic Affairs may withdraw recognition if the service does not meet the requirements laid down in the first or second paragraph, or has no more services for one year. He shall arrange for the publication of the revocation in the Official Journal.


Article 5. Dose gauge data

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  • 2 In the first distribution of a dose-meter and for any major change in use or treatment, the dosimetry service ensures that a statement is made available for the carrier of the dosimeter. the use and handling thereof and that the instruction is at all times retrievable for the carrier and entrepreneur.

  • 3 The entrepreneur pays the costs for the service of the dosimetry service.

  • 4 The entrepreneur lets the exposed worker use the dosage meter for a period of up to five weeks.

  • 5 The entrepreneur ensures, for the purpose of interpreting the radiation dose received, that the exposed worker carries the dose meter appropriately and sets out internal regulations for this, on compliance with which the general Supervising expert, coordinating expert or supervisory expert within the undertaking.

  • 6 The dosimetry service is the processor of the dose data of the exposed worker, for the benefit of the entrepreneur.

  • 7 The dosimetry service carries care for inclusion in the NDRIS, intended in Article 6 , from the data derived from a dosimeter used for the safety and health of an exposed worker.

  • For the implementation of the seventh paragraph, the dosimetry service shall provide the administrator periodically, but not later than two months after its adoption, the dose data derived from the dosimeters provided to exposed workers, in combination with personal data and civil service numbers relating to those employees, in so far as the data is of an A or B employee or an employee using a meter-meter on a voluntary basis.

  • 9 A request for modification of the dose data in the NDRIS intended to Article 6 , shall be submitted to the Director by the economic operator, giving the reasons for the statement.


Article 6. Dose registration in NDRIS

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  • 2 The NDRIS is managed by the Nuclear Research and Consultancy Group, Arnhem location.

  • 3 The NDRIS is also the centralised system for the registration of data of Dutch external workers as referred to in Article 4 (2) of the Directive of the Council of the European Communities, No 90 /641/Euratom of 4 December 1990 on the practical protection of external workers who are at risk of ionising radiation during their work in a controlled area (PbEG L 349/21).

  • 4 For the purpose of the dose registration, the NDRIS contains data on the identity of the dose meter carrier, which in any case includes the name of the letters, date of birth, sex, the civil service number of the dose meter carrier, the the dose data by period and cumulative as well as the name and address of the economic operator.

  • 5 The administrator shall process the dose data provided by a dosimetric service.

  • 6 The administrator shall ensure that the management of the products in question is carefully managed. Articles 87 , 88 and 89 of the Decision said data. It shall also take the necessary measures to prevent any falsification, misuse or unlawful operation of the NDRIS.

  • 7 The administrator shall change the dose data only at the request of the Director. This change takes place in accordance with a protocol, the model of which is included in Annex C This scheme.

  • 8 The administrator reports annually to the Minister of Social Affairs and Employment and the recognised dosimetry service, intended Article 3 , on its work under this scheme in the form of an annual report.


§ 4. Radiation axle port

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Article 7. Model

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As a model of the radiant port, intended in Article 94 of the Decision , it is determined the model, as recorded in Annex D This scheme.


Article 8. Inlay

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  • 1 The radiation axle gate consists of a cover and a inlay for the recording of the dose data.

  • 2 After cessation of operations or work by an external employee, the relevant data shall be recorded on the inlay, and shall be surrendered without delay to the administrator for inclusion in the NDRIS.


Article 9. Costs

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  • 1 The radiation-gate shall be issued by the manager of the NDRIS upon application by the operator against payment of € 110,95. The first inlay is included below.

  • 2 An inlay shall be issued by the manager of the NDRIS upon application by the entrepreneur against payment of € 23,20.

  • 3 The Minister for Social Affairs and Employment shall adjust the amounts set out in paragraphs 1 and 2 each year, starting on 1 January, to the evolution of the index of consumers since the previous adjustment of the amounts and shall ensure that the for publication of the adjustment in the Official Journal.


Article 10. Ownership

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  • 1 The radiation port is and remains the property of the administrator.

  • 2 In the event of loss or loss of the radiant port, the entrepreneur shall inform the administrator without delay.

  • 3 At the expense of the entrepreneur, a new passport is provided, if necessary.


§ 5. Aeroplane crews

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Article 11. Method determination dose

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  • 1 The method referred to in Article 111, first paragraph, part b, of the decision , for determining the effective dose received, consists of bringing the individual relevant flight data from the employee referred to in that article and the dose calculation related to that employee to the third party in question. member mentioned computer program.

  • 2 The individual relevant flight data shall be collected under the responsibility of the expert referred to in paragraph 5, according to a written protocol.

  • 3 The dose calculation is carried out using the computer program CARI-6/6M issued by the Federal Aviation Administration.

  • 4 The determination of the exposure shall be made so that the accuracy of the results can be verified at a later date.

  • 5 The method referred to in paragraph 1 shall be managed by a supervisory expert with the diploma of ionizing radiation at level 5A, supplemented by knowledge of flight crew dosimetry.

  • 6 The entrepreneur ensures that the result of the individual dose calculation referred to in paragraph 1 is sent without delay to the administrator.


§ 6. Warning signs and associated texts

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Article 12. Warning signs

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  • 2 The board, referred to in paragraph 1, shall be at least 7,5 cm wide, unless it is not reasonable in the situation where it is to be applied.


Article 13. Warning sign text

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  • 1 Under or next to the warning sign, intended in Article 12, first paragraph , are located one or more yellow, rectangular signs with a black border with it in black the text:

    • a. 'X-ray radiation', if an appliance is the cause of the possible exposure;

    • b. 'RADIOACTIVE SUBSTANCES', if radioactive substances are the cause of the potential exposure;

    • c. 'MONITORED ZONE', if it is a monitored area;

    • d. 'CONTROLLED AREA', if it is a controlled area.

  • 2 The texts referred to in points (c) and (d) of paragraph 1 shall be accompanied by the text: Dosistempo > 10 μSv/hr if the dose equivalent rate may exceed 10 μSv/h in the zone, if possible.

  • 3 The rectangular board referred to in paragraph 1 shall be at least 7,5 cm wide, unless it is not reasonable in the situation in which it is to be applied.


Article 14. Warning signs on encapsulated sources, devices and source-holders

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  • 2 If the encapsulated sources are concerned, the first paragraph shall not apply to existing sources which are used before 1 March 2002.

  • 4 The first paragraph shall not apply if the dimension of the sealed source is too small for a warning sign recognizable by the naked eye.

  • 6 On the boards, placed on source holders, is Article 12, second paragraph , not applicable, where a source holder has such dimensions as a warning sign in accordance with the requirements of this Regulation. Article 12, first paragraph , with a dimension as referred to in Article 12, second paragraph, together with a rectangular board as referred to in Article 12 Article 13, first paragraph , can not reasonably be placed.

  • 7 The fifth paragraph shall not apply to a source holder who is used at the same time as the source container, provided that the source-holder is in the form of an ADR label.


Article 15. Forbidden sign controlled zone

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  • 2 Under or adjacent to the prohibition sign referred to in paragraph 1, there is a white, rectangular sign with a black border with it in black the text: no access for unauthorised persons.


§ 7. Risk analysis

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Article 16. Risk analysis

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  • 1 The risk analysis shall contain at least the following steps:

    • a. An identification of the risk;

    • b. A calculation of the risk; and

    • c. an evaluation of the risk.

  • 2 The risk analysis shall include a written effect of the steps referred to in paragraph 1, including: Annex E questions included in this scheme are answered consecutively.

  • 3 The effects of the risk analysis shall be recorded by the economic operator in written reporting.


§ 8. Transitional and final provisions

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Article 17. Transitional provision certification approved dosimetry services

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The obligation to certify, intended to Article 4, first paragraph, part c , in respect of a dosimetric service recognised on 1 January 2014, referred to in Article 8, first paragraph, of the Decision , as of 1 January 2017.


Article 18. Transitional dose registration in NDRIS

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By way of derogation from Article 6 (4) , the NDRIS contains only the civil service number of a dose meter carrier, whose dose data will be processed by the administrator after 1 March 2002.


Article 19. Withdrawal arrangements

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Article 20. Entry of

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This arrangement shall enter into force from 1 January 2014.


Article 21. Citation Title

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This scheme is cited as: Order of radiation protection workers 2014.

This arrangement will be set out in the Official Gazette, together with the explanatory notes and annexes.

The Hague, 21 November 2013

The

Minister

of Social Affairs and Employment,

L.F. Asscher


Annex A., Associated with Article 2, first paragraph

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Criteria for radiation doctors to keep the necessary knowledge

  • I. A year on average 3 dayparts have been spent on retraining or retraining on the subject of ionizing radiation. For the five-year tendering period, this means a total of 15 day-to-day parts;

  • II. In addition, one time during the five-year tendering period, a relevant periodic training course of at least two days shall be followed at the level of an education coordinating expert.

    Evidence of participation in the post-or retraining course and the periodic training course shall be attached to the application for renewal of the invitation to tender.


Annex B., Associated with Article 4, second paragraph

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Reporting ex Article 4, second paragraph

The reporting shall provide the following information:

  • 1. The results of the dosimetry carried out in that year.

  • (2) The changes made to the quality manual on the basis of EUR 14852 and any correspondence with the certifying institution thereon.

  • (3) The number of (inter) national surveys to which participated in and a summary of the results of such surveys.

  • 4. The description of the changes to the security system of the data and the precautions taken to prevent the loss of data.

  • 5. Any bottlenecks.

  • 6. Any complaints received and the treatment thereof.

  • 7. Any change in the division of tasks within the service and the changes in the composition of the board.

  • 8. The (financial) annual report of the organization of the service.


Annex C. Associated with Article 6, seventh paragraph

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Change Dose Data protocol

There are unforeseen circumstances in which the dose determined with the person dosimeters, does not reflect the effective dose correctly. In such cases, the entrepreneur is required to make a request to have the dose recorded in NDRIS modified in accordance with the procedure described in the accompanying schedule.

In case of an error of a technical nature at the reading of the person dosimeter, which makes the dose meter rash incorrect, the dose metrical service may change through the operator of the NDRIS without the intervention of the Inspectorate SZW. of the dose data. The procedure described here then does not apply.

Annex 252671.png Schedule Modification of dose data in the NDRIS

Annex D, associated with Article 7 and 8, 1st Member

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Model radiant port

Annex 252672.png Annex 252673.png Annex 252674.png

Annex E., Associated with Article 16, second paragraph

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Steps risk analysis

A risk analysis identifies the following steps: Risk identification, risk calculation, and risk assessment. In a written report, these steps shall be elaborated and the following questions shall also be answered.

  • 1. Risk identification:

    • • Have all sources of ionizing radiation and their properties been inventoried?

    • • What actions are taking place with these sources? Split acts in instalments, if necessary, in order to specify the exposure risks.

    • • Where do these acts take place?

    • • What measures (technical and organisational) have been taken to limit the exposure?

    • • What kind of exposure are the subject?

    • • How many (part) actions take place on an annual basis, and how many/what persons can be exposed to that?

    • • What 'anticipated unintended events' can contribute to the potential exposure?

  • 2. Risk calculation:

    • • What annual dose is to be expected for the persons concerned on the basis of a responsible estimate of the regular and potential exposure?

      In this respect, an understanding should be provided to:

      • -the effect of personal protective equipment,

      • -the possibility of preventing the 'anticipated unintended events'.

  • 3. Risk assessment:

    • • The legislation shall be complied with in respect of:

      • -the classification of the persons concerned as an 'worker' or 'exposed worker' (category A or B) on the basis of the annual dose calculated 1

      • -the layout of spaces in 'controlled zone' or 'monitored zone',

      • -the basic principle of ALARA,

      • -dose limits,

      • -the need to take additional measures?