Pharmaceutical Process Scale- Up. A Plan for Total Quality Control from Manufacturer to Customer
โ Scribed by Levin M. (ed.)
- Publisher
- M.Dekker
- Year
- 2001
- Tongue
- English
- Leaves
- 589
- Edition
- 5ed.
- Category
- Library
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Status and Applicability of U.S. Regulations: Current Good Manufacturing Practices in Manufacturing, Processing, Packaging, and Holdings of DrugsFinished Pharmaceuticals: General Provisions (Subpart A)Organization and Personnel: (Subpart B)Buildings and Facilities: (Subpart C)Equipment: (Subpart D)
<br> Content: Status and Applicability of U.S. Regulations: Current Good Manufacturing Practices in Manufacturing, Processing, Packaging, and Holdings of DrugsFinished Pharmaceuticals: General Provisions (Subpart A)Organization and Personnel: (Subpart B)Buildings and Facilities: (Subpart C)Equipment
Highlighting key issues and differences among GMPs of Europe, Canada, and the WHO, this reference examines US law and governmental policy affecting domestic and multinational pharmaceutical manufacturing. The book recommend pragmatic ways to interpret and comply with FDA CGMP regulation and related
This book recommends pragmatic ways to interpret and comply with FDA CGMP regulation and related criteria, they focus on geographical redistribution of manufacturing facilities, adaptation to disparate human resources, and others.
Highlighting key issues and differences among GMPs of Europe, Canada, and the WHO, this reference examines US law and governmental policy affecting domestic and multinational pharmaceutical manufacturing. The book recommend pragmatic ways to interpret and comply with FDA CGMP regulation and related