ML19224C640

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Revised QA Program for Industrial Radiography
ML19224C640
Person / Time
Site: 07100066
Issue date: 05/04/1979
From:
CERTIFIED TESTING LABORATORIES, INC.
To:
Shared Package
ML19224C638 List:
References
NUDOCS 7907060011
Download: ML19224C640 (3)


Text

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CERTIF IED TEST ING LABORATORIES. INC.

10 CFR PART 71 OA PROGRAM FOR INDUSTR AL RAD I OGRAPHY 1.

Organization The final res pons ibi l it y for the Qua l i t y Assurance (QA)

P rog ra m f o r Pa r t 71 Requi rements res ts with Cert i fied Tes t ing Labora tor ies, Inc.

Des i gn and Fabrica t ion s ha l l not be conducted under this QA Program.

The QA Program is implemented using the follaving organization:

PRESIDENT l

Corpora te Level lil I

Leve l 11 Shipping Level i T ra i nees The Radia t ion Sa fet y Of f ice r is res pons i b le for overa ll a dmi n i s t ra t ion of the progra m, t ra i n i ng and ce rt i f i ca t ion,

document con t a l, a nd a ud i t '. ng.

T he Ra d iog ra phe rs a re res pons ib le for ha nd l i ng, storing, s hi pping, i ns pect ion, tes t and ope rat i ng s ta tus and record keeping.

2 Qua l it y Assurance P rog ram T he ma na geme n t of Cert i f ied Tes t ing Labora tories, Inc.

es tab l is hes and implements this QA P rog ra m.

T ra i n i ng, prior to engagement, for a ll QA f unct ions is requi red according to

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2 Qua l i t y Ass ura nce Prog ra m (continued) written procedures.

QA Program rev is ions wi l l be made according to written procedu res wi t h ma nagement a pprova l.

The QA Program will ensure that a ll defined QC proccdures,

engineering procedures, and s peci fic provis ions of the pa ckage des i gn a pprova l a re sat is fied.

The QA Program wi l l emphas ize cont rol of the cha racteris t ics of the pa cka ge which a re cr i t ica l to sa fet y.

The Radiat ion Sa fet y Of f icer s ha l l assure tha t all ra d i o -

a ct ive na te r ia l s hi ppi ng pa ckages a re des i gned a nd

.T inu-factured under a QA Program approved by Nuclear Regulatory Commission for all pa cka ges des igned or fabricated a f ter the ef fect ive data of the QA Program.

This req u i remen t can be sa t is f ied by rece iving a cert ification to this ef fect from t he na nu f a ct u re r.

3 Document control All documents related to a specific shipping package will be controlled through the use of written procedures.

All document changes will be pe rformed accord ing to wr i t ten procedures a pproved by nanagement.

The Ra d ia t i on Sa fet y Of f i ce r s ha l l i ns u re t ha t a l l QA f unct ions a re conducted in accordance with the la tes t a pp l i cab le changes to these documen ts.

4.

Handling Storage and Shipping Wri t ten sa fet y procedures conce rning the handl ing, s to ra ge and shipping of packages for certa in s pecia l form radio-a ct ive no ter ia l wi l l be followed.

S ments will not be nu de unless all tests, ce rt i f i ca t ions, a cceptances, a nd finai inspect ions have been completed.

Work instructions will be provided for handling, s torage, and s hi pping ope ra t i ons.

Ra d i og ra phy pe rs onne l s ha l l pe r form t he cr i t i ca l ha nd l ing,

s torage and s hi pping operat ions.

5 I ns pe ct i on, Test and operat ing Status i ns pect ion, tes t and ope ra t ing s ta t us of pa ckages for certa in s pecia l form radioa ct ive mate ria l wil l be indi-ca ted and controlled by written procedures.

Status will be i nd i cated by ta g, labe l, ma rki ng o r log entry.

Status o f nonconf ormi ng pa rts or pa cka ges w i ll be pos i t ive l y ma i n-ta ined by written procedures.

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5 I ns pe ct i on, Tes t and Opera t ing S ta tus (continued)

Radiogra phy pe rsonne l sia 11 perform the regulatory requi red ins pect ions and tes ts in accordance with written procedures.

The Radia t ion Sa fet y Of f i ce r s ha l l ens ure t ha t these func-t ions a re performed.

6.

Q ua l i t y As s u ra n ce Records Records of pa ckage a pprova ls (including references and d raw i ngs ), p rocu reme n t, i ns pe ct i ons, tes ts, ope ra t i ng logs, audit res ul ts, pe rs onne l t ra i n i ng a nd q ua l i f i ca t ions a nd reco rds o f s h i pments w i l l be ma i nta i ned.

Des cr i pt ions of equipment and written procedu res w i l l a ls o be ma i nta i ned.

These records w i l l be ma i nta i ned in accordance with written procedures.

The records will be ident i f iab le and ret r ievab le.

A list of these records, w i t h t he i r s torage l oca t ions, w i l l be na i nta ined by t he Radia t ion Safety Officer.

7 Audits Es tablished schedules of audits of the QA Program will be pe rformed us ing wri t ten check lists.

Resu l ts of audi ts w i l l be na i nta i ned and re po r te d t o na na geme n t.

Audit reports wi l l be eva luated and deficient a reas corrected.

The audi ts w i l l be de pendent on the sa fet y s igni f icance of the act iv i t y be ing audited, but each activit y will be audited at leas t once per yea r.

Audit reports will be na i nta ined as pa r t of t he qua l i t y ass ura nce records.

Membe rs o f t he a ud i t team s ha l l ha ve no res pons i b i l i t y in the activity being audited.

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