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Consenting Process for Radiation Facilities - Atomic Energy ...

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3.3.3 Layout and Constration Approval<br />

The consent <strong>for</strong> construction involves review of the safety aspects as presented<br />

in the preliminary safety analysis report (PSAR) <strong>for</strong> the facility. PSAR should<br />

contain identification of potential safety hazards to equipment and personnel<br />

and the manner in which potential hazards and risks will be minimised.<br />

Mitigation of hazards can be accomplished through design safety features,<br />

safe operating procedure and training and administrative controls. Analysis<br />

of design or postulated emergency conditions, including those due to natural<br />

or disruptive factors should be provided in the PSAR. PSAR should conclude<br />

with justification <strong>for</strong> adequacy of safety measures. In addition applicant is<br />

required to submit civil engineering drawings, shielding design, baseline data<br />

on radiological parameters, ventilation system and design features of access<br />

control system. The construction schedule and QA manual <strong>for</strong> design and<br />

construction should also be submitted. The <strong>for</strong>mat <strong>for</strong> QA manual should be<br />

as per Appendix 4F. Job hazard analysis report identifying the hazards and<br />

mitigation measures <strong>for</strong> major jobs having potential <strong>for</strong> accident should be<br />

made available at the facility <strong>for</strong> various construction activities.<br />

The <strong>for</strong>mat <strong>for</strong> PSAR is given in Appendix 4B and 4D. The <strong>for</strong>mat <strong>for</strong><br />

application <strong>for</strong> construction consent is given in Annexure 8.<br />

After the completion of construction of building structures, the facility should<br />

prepare construction completion certificate (CCC) documents covering asbuilt<br />

design features along with justification of modifications made from the<br />

intended design (if any). This should be available with the facility be<strong>for</strong>e<br />

start of commissioning.<br />

3.3.4 Commissioning<br />

The consent <strong>for</strong> commissioning may be issued in several interim stages and<br />

will vary widely depending on the type of the research facility. The applicant<br />

should submit <strong>for</strong> review, the specifications of all systems, design manual,<br />

facility layout with details of site and building features, schedule <strong>for</strong><br />

commissioning and commissioning procedures (CPs). The acceptance test<br />

report (ATR) needs to be submitted as per Appendix 4C. Apart from this,<br />

emergency preparedness procedures (EPP) and radiation protection manual<br />

(RPM), which should be as per AERB radiation protection manual (no separate<br />

<strong>for</strong>mat is given here) should also be submitted. The applicant is required to<br />

submit operator training and authorisation report. Availability of qualified<br />

manpower including approved radiological safety officer (RSO) during<br />

commissioning should be ensured. The <strong>for</strong>mat <strong>for</strong> application of RSO is given<br />

in Annexure 9.<br />

The applicant is also required to submit quality assurance manual <strong>for</strong><br />

commissioning and operation and the <strong>for</strong>mat of the same is given in<br />

24

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