13.01.2015 Views

Consenting Process for Radiation Facilities - Atomic Energy ...

Consenting Process for Radiation Facilities - Atomic Energy ...

Consenting Process for Radiation Facilities - Atomic Energy ...

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Applicant submits to AERB an application <strong>for</strong> obtaining the regulatory consent<br />

<strong>for</strong> routine operation along with final safety analysis report (FSAR) in a<br />

standard <strong>for</strong>mat given in Appendices which is applicable <strong>for</strong> facilities such<br />

as gamma radiation processing facility, high energy particle accelerators used<br />

<strong>for</strong> research and industrial applications (above 10 MeV), medical cyclotron<br />

facility and integrated facility <strong>for</strong> radiation technology.<br />

Based on the review of an application <strong>for</strong> obtaining the Regulatory Consent<br />

<strong>for</strong> routine operation along with final safety analysis report (FSAR) in a<br />

standard <strong>for</strong>mat, the Consent <strong>for</strong> routine operation is issued specifying a<br />

validity period after which it may be renewed on the basis of a regulatory<br />

review of the facility <strong>for</strong> safe per<strong>for</strong>mance. The procedure <strong>for</strong> renewal of<br />

Consent <strong>for</strong> routine operation is given in subsection 2.10.<br />

During regular operation of the facility, safety reviews are carried out by the<br />

AERB periodically to ensure that the facility is being operated in accordance<br />

with the stipulations made in the Consent and also the procedures outlined in<br />

the documents submitted to AERB. In addition the facility is required to<br />

submit periodic safety status reports to AERB.<br />

Modification to the plant design and operating procedures, having a bearing<br />

on safety and relevant to the <strong>Consenting</strong> process, requires approval by AERB.<br />

Modification may also include augmentation, expansion, life extension, etc.<br />

Relevant documents on the modification, together with justification and safety<br />

implication, should be submitted to AERB <strong>for</strong> safety review and assessment.<br />

2.4.6 Consent <strong>for</strong> Decommissioning/Disposal<br />

At the end of the service-life of the radiation facility, it is obligatory on the<br />

part of the Licensee to undertake decommissioning and safe disposal of spent/<br />

disused sources. A report on the decommissioning procedures should be<br />

submitted to AERB. After review of the safety aspects Consent may be issued<br />

<strong>for</strong> decommissioning of the radiation facility and safe disposal of the<br />

radioactive waste generated, if any, with certain stipulations to be fulfilled<br />

by the consentee.<br />

2.4.7 Renewal of Consent <strong>for</strong> Operation/Type Approval/RSO<br />

The application <strong>for</strong> renewal of regulatory Consent <strong>for</strong> operation of radiation<br />

facilities is processed on the basis of the review of the periodic safety status<br />

report and report on any unusual occurrence in the facility. Prior to renewal,<br />

inspection of the facility is carried out, if necessary based on the review of<br />

the safety status reports to ensure that the operation of the facility is in<br />

con<strong>for</strong>mity to its intended manner. The application <strong>for</strong>mats <strong>for</strong> renewal of<br />

regulatory Consent <strong>for</strong> operation of radiation facility or type approval of<br />

devices/ equipment or RSO approval are same as the application <strong>for</strong>mat used<br />

6

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!