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Consenting Process for Radiation Facilities - Atomic Energy ...

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3.17.2 Layout Plan Approval<br />

The layout plan <strong>for</strong> RIA laboratory has to be approved by AERB. The<br />

application <strong>for</strong>mat <strong>for</strong> obtaining the layout plan approval is issued in<br />

Annexure 46.<br />

3.17.3 Commissioning and Operation<br />

Prior to seeking Registration <strong>for</strong> RIA laboratory, the applicant should have<br />

the RIA lab and associated facilities constructed as per plan approved by<br />

AERB. The RIA laboratory should have, be<strong>for</strong>e commissioning<br />

(i)<br />

(ii)<br />

Technician with prescribed training, and<br />

Necessary laboratory accessories.<br />

AERB may grant Registration <strong>for</strong> the facility on the basis of the review of the<br />

application <strong>for</strong>m <strong>for</strong> Registration/NOC <strong>for</strong> RIA facility, the <strong>for</strong>mat of which<br />

is given in Annexure 47. The NOC <strong>for</strong> import of radioactive material is a<br />

kind of consent issued to enable the consentee to procure radioactive material<br />

<strong>for</strong> the use in the approved RIA facility. This is given as per Annexure 48.<br />

3.17.4 Lead Time <strong>for</strong> Submission/Availability of Documents<br />

The lead time <strong>for</strong> submission of documents at any stage of consenting process<br />

is 30 days be<strong>for</strong>e the desired date of consent and the documents should be<br />

complete in all respects <strong>for</strong> review by AERB.<br />

3.18 Consent/Type Approval<br />

3.18.1 Type Approval of Sources, Equipment, Devices and Packages<br />

The AERB against an application complete in all respects grants Type<br />

Approval <strong>for</strong> the sources, equipment, devices and packages after detailed<br />

review. The pre-requisites <strong>for</strong> approval of indigenously manufactured items<br />

include submission of:<br />

(i)<br />

(ii)<br />

(iii)<br />

Technical specifications, design and other relevant in<strong>for</strong>mation<br />

Quality assurance (QA) programme, wherever applicable, as given<br />

in national/international standards<br />

Test report meeting the relevant specifications in accordance with<br />

standards approved by AERB or National/International standards<br />

followed.<br />

AERB may carry out review of the test procedures on which the in<strong>for</strong>mation<br />

is provided in the Application.<br />

In the case of imported equipment and devices, AERB may grant ‘No<br />

Objection Certificate (NOC)’ <strong>for</strong> import based on an application submitted<br />

74

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