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Document Initiation, Revision, Distribution and Control
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Item Number: NWRR0101
A procedure that describes creation, revision, review, approval, filing, archiving, and distribution of quality documents. This procedure applies to all Manufacturing documents, Standard Operating Procedures, Test Methods, and Specifications required in support of products regulated by the FDA. This is a 15-page document, including five attachments (Document Change Request, Document Identification Numbers, Document Change Request Log, Document Formats, and Subsection Description), assigns responsibility for each step of the procedure.
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