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Consenting Process for Radiation Facilities - Atomic Energy ...

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3.5.2.5 Commissioning and Operation<br />

Be<strong>for</strong>e the grant of commissioning and operation licence, the Applicant is<br />

required to<br />

(i)<br />

(ii)<br />

(iii)<br />

Evaluate the per<strong>for</strong>mance of the type-approved telegamma unit and<br />

prepare acceptance test report and submit to AERB.<br />

Prepare and implement the quality assurance programme<br />

Prepare and implement the <strong>Radiation</strong> Protection Manual as per<br />

Appendix 7E.<br />

These documents would be reviewed by AERB prior to grant of Licence <strong>for</strong><br />

commissioning and operation.<br />

The application <strong>for</strong>mat <strong>for</strong> obtaining consent <strong>for</strong> commissioning and operation<br />

of the medical linear accelerator is given in Annexure 22<br />

In case the medical linear accelerator is not type approved, AERB considers<br />

<strong>for</strong> type approval of the medical linear accelerator unit separately as explained<br />

in subsection 3.18.1.<br />

Prior to seeking Regulatory approval <strong>for</strong> commissioning and operation, the<br />

Consentee should have:<br />

(i)<br />

(ii)<br />

(iii)<br />

(iv)<br />

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

physicist, RSO, and radiation therapy technologist;<br />

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

Protection level and therapy level dosimeters<br />

Dosimetry accessories including radiation field analyser.<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.<br />

The Consentee should ensure that<br />

(i)<br />

(ii)<br />

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

and depths <strong>for</strong> all beam energies, and<br />

measurement of radiation levels at all occupied locations<br />

are carried out at the time of commissioning and periodically or whenever<br />

repairs are carried out that is likely to affect the dosimetric and radiation<br />

safety per<strong>for</strong>mance of the unit.<br />

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

the end of each calendar year. Unusual occurrences should be promptly<br />

reported within 24 hours and this should be followed by a detailed report.<br />

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

40

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