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Good Manufacturing Practice finished dosage forms

Good Manufacturing Practice. The GMPs were issued by the U.S. FDA in 1978 to provide minimum quahty standards in the production of pharmaceuticals (qv) for the finished dosage form as well as their ingredients. The standard has been updated periodically. [Pg.372]

Exhibit 10.13 Packaging and Labeling of APIs and Intermediates (ICH (1997) Guide for API Good Manufacturing Practice). Also Including Finished Dosage Forms... [Pg.278]

See other pages where Good Manufacturing Practice finished dosage forms is mentioned: [Pg.275]    [Pg.637]    [Pg.286]    [Pg.72]    [Pg.73]    [Pg.55]    [Pg.1785]    [Pg.3271]    [Pg.125]    [Pg.430]    [Pg.515]   
See also in sourсe #XX -- [ Pg.348 , Pg.349 , Pg.350 , Pg.351 ]



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