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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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