Consenting Process for Radiation Facilities - Atomic Energy ...
Consenting Process for Radiation Facilities - Atomic Energy ...
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 />
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