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Salvaged drug products

This system assures overall compliance with cGMPs and internal procedures and specifications. The system includes the quality control unit and all of its review and approval duties (e.g. change control, reprocessing, batch release, annual record review, validation protocols, and reports, etc.). It includes all product defect evaluations and evaluation of returned and salvaged drug products. [Pg.247]

A review of complaints, recalls, returned or salvaged drug products, and investigations conducted under 211.192 for each drug product. [Pg.62]

Subpart E Control of Components and Drug Product Containers and Closures Subpart F Production and Process Controls Subpart G Packaging and Labeling Control Subpart H Holding and Distribution Subpart I Laboratory Controls Subpart J Records and Reports Subpart K Returned and Salvaged Drug Products... [Pg.637]

TABLE 26 Contents of Snbpart of Part 211 of U.S. GMP Regulations Covering Returned and Salvaged Drug Products [7]... [Pg.158]

K Return and salvaged drug products Batch reprocessing... [Pg.19]

Control of nonconforming products Returned and salvaged drug products... [Pg.3939]

Subpart K—Returned and Salvaged Drug Products 211.204 Returned drug products. [Pg.718]

See other pages where Salvaged drug products is mentioned: [Pg.215]    [Pg.13]    [Pg.73]    [Pg.100]    [Pg.82]    [Pg.20]    [Pg.23]    [Pg.24]    [Pg.120]    [Pg.121]    [Pg.157]    [Pg.157]    [Pg.158]    [Pg.158]    [Pg.158]    [Pg.203]    [Pg.519]    [Pg.1947]    [Pg.521]    [Pg.216]    [Pg.210]    [Pg.706]    [Pg.724]    [Pg.87]    [Pg.12]    [Pg.130]   
See also in sourсe #XX -- [ Pg.1946 ]



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