Current Good Manufacturing Practices: Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise R

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	New		3rd Party New		3rd Party Used
Latest	$42.99	Latest	$35.12	Latest	$37.10
Highest	$42.99 Oct 16, '15	Highest	$37.32 May 7, '14	Highest	$40.18 Nov 5, '14
Lowest	$38.69 Jul 8, '13	Lowest	$28.22 Feb 19, '16	Lowest	$10.82 Feb 3, '16
Average	$41.09	Average	$34.48	Average	$29.41
Added	Apr 24, 2013	Added	Apr 24, 2013	Added	Apr 24, 2013

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Product Description

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

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Amazon > Books > Subjects > Education & Reference > Writing, Research & Publishing Guides > Research

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