Good Clinical Practice - Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise Reference; Volume 2, Guidance (Paperback)

Selected FDA GCP/Clinical Trial Guidance Documents Grouped by Topic: * FDA Overview and Orientation * Introduction to GCP * Part I: General * Part II: Institutional Review Boards (IRBs) and Informed Consent * Part III: Drugs and Biologics * Part IV: Medical Devices * Part V: Manufacturing Requirements for Investigational Products * Part VI: Electronic Data Reference Tools * Part VII: Combined Glossary and Index for all Quality Guidance Documents

General

Imprint:	Pharmalogika
Country of origin:	United States
Release date:	October 2010
First published:	October 2010
Authors:	Mindy J. Allport-Settle
Dimensions:	235 x 191 x 38mm (L x W x T)
Format:	Paperback - Trade
Pages:	752
ISBN-13:	978-0-9821476-8-9
Categories:	Books > Medicine > General issues > Medical equipment & techniques > Medical research
LSN:	0-9821476-8-6
Barcode:	9780982147689

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