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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and supporting heavy structures. Further, presence of any ammunition dumps,<br />
and storage of inflammable and toxic substances in the vicinity are also<br />
considered.<br />
Basement may be an ideal site <strong>for</strong> location since the earth provides natural<br />
and effective shielding. Alternatively, medical cyclotrons may be located<br />
ground level as well. The medical cyclotron installations <strong>for</strong> the purpose of<br />
commercial radioisotope production and distribution should be housed in<br />
industrial areas. The application <strong>for</strong>mat <strong>for</strong> obtaining regulatory clearance<br />
<strong>for</strong> site approval is given in Annexure 12.<br />
3.4.1.3 Layout Plan, Design/Construction Approval<br />
The medical cyclotron shall be housed in a room with adequate shielding.<br />
<strong>Radiation</strong> areas and electrical high voltage areas need adequate isolation and<br />
access control. The design should incorporate safe cable routing, segregation<br />
of power and signal cables and provision of barriers to prevent fire. Firepropagating<br />
material should not be in the vicinity of electrical joints.<br />
The layout of the medical cyclotron facility shall be approved by AERB. As<br />
part of construction/layout plan approval by AERB a preliminary safety<br />
analysis report (PSAR) <strong>for</strong> medical cyclotron facility should be submitted.<br />
The PSAR <strong>for</strong> medical cyclotron facility should contain the details as per the<br />
Appendix 5B.<br />
The regulatory clearance <strong>for</strong> construction is granted after design safety review<br />
and layout plan approval and safety analysis of the installation, stipulating<br />
the checkpoints, hold points and QA requirements. The AERB may inspect<br />
the facility while under construction to verify whether the construction is as<br />
per design. The consentee is required to submit periodic reports on quality<br />
assurance to AERB. Installation of equipment, and preliminary tests on various<br />
systems are to be carried out in a phased manner as per the checkpoints. The<br />
application <strong>for</strong> layout plan and construction approval of medical cyclotron<br />
facility is given in Annexure 13. The QA manual <strong>for</strong> construction should be<br />
prepared and maintained by the facility and should be as per the <strong>for</strong>mat<br />
given in Appendix 5F.<br />
3.4.1.4 Commissioning and Operation<br />
For granting licence <strong>for</strong> commissioning, the AERB evaluates the system<br />
per<strong>for</strong>mance and the shielding adequacy of the installation. Prior to seeking<br />
permission, the applicant should have<br />
(i)<br />
(ii)<br />
Qualified and trained manpower-operators, radio pharmacist and<br />
RSO Level-III<br />
Personnel monitoring devices <strong>for</strong> all radiation workers<br />
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