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Consenting Process for Radiation Facilities - Atomic Energy ...

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The application <strong>for</strong>mat <strong>for</strong> getting Licence <strong>for</strong> commissioning and operation<br />

of the telegamma therapy unit is given in Annexure 22.<br />

In case the unit is not type approved, AERB considers separately <strong>for</strong> type<br />

approval of the telegamma therapy unit as explained in subsection 3.18.1.<br />

Prior to seeking regulatory clearance <strong>for</strong> commissioning and operation, the<br />

Consentee should have:<br />

(i)<br />

(ii)<br />

(iii)<br />

(iv)<br />

(v)<br />

Qualified and trained manpower - radiation oncologist, medical<br />

physicist, RSO Level-III, and radiation therapy technologist<br />

Personnel monitoring devices <strong>for</strong> all workers<br />

Protection level and therapy level dosimeters<br />

Dosimetry accessories<br />

<strong>Radiation</strong> zone monitor.<br />

It is also advisable that a treatment planning system and a treatment simulator<br />

are available <strong>for</strong> proper treatment planning and <strong>for</strong> treatment simulation. Also,<br />

the Consentee shall obtain a regulatory clearance <strong>for</strong> the procurement of<br />

radiation sources <strong>for</strong> radiation therapy <strong>for</strong> which the application <strong>for</strong>mat is<br />

given in Annexure 21.<br />

The Consentee should ensure that:<br />

(i)<br />

(ii)<br />

calibration of radiation beam output <strong>for</strong> all field sizes, dosimetry <strong>for</strong><br />

all field sizes and depths, and<br />

radiation level measurements at all occupied locations<br />

are carried out at the time of commissioning. They are further carried out<br />

periodically or whenever repairs which are likely to affect the dosimetric<br />

and radiation safety per<strong>for</strong>mance of the unit are carried out. The QA aspects<br />

to be carried out during operation are spelt out in detail in AERB safety code<br />

titled ‘<strong>Radiation</strong> Therapy Sources, Equipment and Installations’, [AERB/<br />

RF-MED/SC-1 (Rev. 1), 2011].<br />

The Consentee is required to submit annual safety status report to AERB.<br />

Unusual occurrences should be promptly reported within 24 hours and this<br />

should be followed by a detailed investigation report. AERB may conduct<br />

inspection <strong>for</strong> the radiation facility as and when required.<br />

The Consentee shall arrange to constitute a Local Safety Committee with the<br />

Head of the institution as Chairman and the RSO as Member Secretary, to<br />

review the safety status of all the radiation facilities in the institution. The<br />

Committee may also include the service engineer as a member. The minutes<br />

of the meetings and the action taken reports shall be available <strong>for</strong> inspection<br />

by AERB.<br />

37

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