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Drug stability Good Manufacturing Practice

Code of Federal Regulations, Title 21, Food and Drugs, Part 211, Current good manufacturing practice for finished pharmaceuticals, Subpart I, 211.166 Stability Testing. [Pg.173]

Drug Stability Principles and Practices, Third Edition, Revised and Expanded, edited by Jens T. Carstensen and C. T. Rhodes Containment in the Pharmaceutical Industry, edited by James P. Wood Good Manufacturing Practices for Pharmaceuticals A Plan for Total Quality Control from Manufacturer to Consumer, Fifth Edition, Revised and Expanded, Sidney H. Willig... [Pg.550]

Good Manufacturing Practices for Stability Testing of Pharmaceutical Products Containing Well Established Drug Substances in Conventional... [Pg.3]

Chapter 2 introduces the critical current Good Manufacturing Practices (cGMP) regulations that are applicable to a stability program. It describes different types of stability studies to support the drug development process and discusses the GMP requirements surrounding the stability sciences. [Pg.402]

See other pages where Drug stability Good Manufacturing Practice is mentioned: [Pg.450]    [Pg.249]    [Pg.139]    [Pg.580]    [Pg.697]    [Pg.146]    [Pg.316]    [Pg.57]    [Pg.94]    [Pg.1580]    [Pg.1685]    [Pg.1692]    [Pg.1785]    [Pg.2487]    [Pg.442]    [Pg.35]    [Pg.33]    [Pg.149]    [Pg.302]    [Pg.184]    [Pg.175]    [Pg.110]    [Pg.1]    [Pg.17]    [Pg.138]    [Pg.36]    [Pg.362]    [Pg.2721]    [Pg.3635]    [Pg.215]    [Pg.463]    [Pg.518]    [Pg.545]    [Pg.116]    [Pg.243]    [Pg.111]    [Pg.134]   
See also in sourсe #XX -- [ Pg.309 ]



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