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Consenting Process for Radiation Facilities - Atomic Energy ...

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plan and obtain the necessary consent. RSO is required to submit to AERB,<br />

report on safe decommissioning, disposal of radioactive wastes, and personnel<br />

doses received during the decommissioning operation.<br />

3.10.1.6 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 />

3.10.2 In-vivo Nuclear Medicine Diagnostic Facility<br />

3.10.2.1 General<br />

A small quantity of radionuclides such as 99m Tc, 131 I, 201 Tl and 18 F in a <strong>for</strong>m<br />

that can be readily absorbed by an organ/tissue of interest is administered by<br />

a chosen route (e.g. intravenous/oral). Preparation of radiopharmaceuticals,<br />

dose administration, imaging and waste collection and disposal should be<br />

done by persons qualified and specially trained in these aspects as stipulated<br />

by AERB.<br />

3.10.2.2 Site and Layout Plan Approval<br />

While planning the nuclear medicine diagnostic facility, areas <strong>for</strong> source<br />

storage, source preparation and dose administration, and radioactive waste<br />

storage and disposal, should be segregated, graded in terms of activity level,<br />

and access controlled accordingly. The Floor must be lined and walls painted<br />

with special materials to facilitate easy decontamination. The site and layout<br />

plan of the laboratory should be approved by AERB. The application <strong>for</strong><br />

approval of site and layout plan <strong>for</strong> nuclear medicine facility is given in<br />

Annexure 33a.<br />

3.10.2.3 Construction<br />

The construction of the nuclear medicine diagnostic facility can be started<br />

after obtaining layout plan approval and no separate regulatory clearance is<br />

required <strong>for</strong> construction. However, AERB may inspect the facility while<br />

under construction to verify whether the construction is as per approved design<br />

and layout.<br />

3.10.2.4 Commissioning and Operation<br />

Prior to seeking Authorisation <strong>for</strong> commissioning, the Consentee should have:<br />

(i)<br />

(ii)<br />

(iii)<br />

qualified and trained manpower - Nuclear Medicine Physician,<br />

Nuclear Medicine Technologist and RSO Level-II,<br />

personnel monitoring devices <strong>for</strong> all workers,<br />

protection level survey meters, contamination monitors,<br />

57

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