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Consenting Process for Radiation Facilities - Atomic Energy ...

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3.5.1.6 Decommissioning/Disposal<br />

Consent from AERB should be obtained <strong>for</strong> decommissioning when the<br />

telegamma unit is no longer to be used. The Consentee should arrange to<br />

remove the radioactive source and depleted Uranium, if present, and return<br />

them to the supplier <strong>for</strong> safe disposal. For the above, the Consentee should<br />

obtain an Authorisation from AERB <strong>for</strong> transfer/disposal of radioactive waste<br />

to the authorised waste management agency. The application <strong>for</strong>mat <strong>for</strong><br />

obtaining the said Authorisation <strong>for</strong> safe disposal of radioactive waste is given<br />

in Annexure 50. The consentee is required to submit a report to AERB on<br />

completion of decommissioning, safe disposal of sources and personnel doses<br />

received during decommissioning operations.<br />

3.5.1.7 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 60 days be<strong>for</strong>e the desired date of consent provided the application is<br />

complete in all respects <strong>for</strong> review by AERB.<br />

3.5.2 Medical Linear Accelerator Facility<br />

3.5.2.1 General<br />

Linear accelerators, betatrons and microtrons are capable of providing electron<br />

beams in the range of 6 MeV to 42 MeV and/or photon beams in the range of<br />

4 MV to 25 MV <strong>for</strong> treatment of deep/shallow tumours. In betatrons and<br />

microtrons, the electron beams get accelerated in several orbits by a magnetic<br />

field. The regulatory procedures <strong>for</strong> units based on Medical Accelerator such<br />

as tomotherapy, cyberknife, intraoperative unit or any other similar unit is<br />

same as those of medical linear accelerator (MLA) facility.<br />

Check sources are used in Radiotherapy facility <strong>for</strong> checking the functionality<br />

of the radiation measuring equipment such as secondary standard dosimeters.<br />

The regulatory procedure to be followed <strong>for</strong> procurement of these sources is<br />

same as that <strong>for</strong> discrete brachytherapy sources (see subsection 3.8.4).<br />

3.5.2.2 Site and Layout Plan Approval<br />

The room housing the accelerator should preferably be located at one end of<br />

the hospital and contiguous with other radiation therapy facilities. Basement<br />

is desirable site <strong>for</strong> location of accelerator facilities since the earth can <strong>for</strong>m<br />

a cheap and effective shielding. Since high voltages are involved, the site<br />

should be free from flooding and high moisture in air. Dust load should be<br />

negligible to prevent electrical sparking. In addition, ventilation should be<br />

taken care of. It shall be ensured that the site can take the heavy shielding<br />

load of the accelerator unit.<br />

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