Current Good Manufacturing Practices - Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise Reference (Paperback)

FDA Regulations and Associated Guidance Documents: - Part 11 Electronic Records; Electronic Signatures - Part 26 Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and the European Community - Part 200 Drugs General - Part 207 Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution - Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs - Part 211 Current Good Manufacturing Practice For Finished Pharmaceuticals - Part 600 Biological Products: General - Part 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices - Part 820 Quality System Regulation Reference Tools: - Glossaries combined in one location - GMP Keyword Index for 21CFR211 - Combined Index for all documents

General

Imprint:	CreateSpace
Country of origin:	United States
Release date:	September 2009
First published:	September 2009
Authors:	Mindy J. Allport-Settle
Dimensions:	229 x 152 x 33mm (L x W x T)
Format:	Paperback - Trade
Pages:	634
ISBN-13:	978-1-4495-0523-3
Categories:	Books > Reference & Interdisciplinary > Encyclopaedias & reference works > Reference works > General
LSN:	1-4495-0523-6
Barcode:	9781449505233

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