Good laboratory practice regulations / edited by Sandy Weinberg.
Material type:
TextSeries: Drugs and the pharmaceutical sciences ; v. 124Publisher: New York : Marcel Dekker, 2003Edition: Third editionDescription: x, 244 pages. ; 23 cmContent type: - text
- unmediated
- volume
- 0824708911 (alk. paper)
- 615.19072 21 G
| Item type | Current library | Collection | Call number | Status | Date due | Barcode | |
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Books
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Main library A11 | Pharmacy ( Pharmaceutical Technology ) | 615.19072 G (Browse shelf(Opens below)) | Available | 00000696 | ||
Books
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Main library A11 | Pharmacy ( Pharmaceutical Technology ) | 615.19072 G (Browse shelf(Opens below)) | Available | 00000697 |
Includes bibliographical references (p. 229-237) and index.
Historical Perspective, Jean M. Taylor and Gary C. SteinFDA/ GLP Regulations, Wendell A. PetersonApplying 21 CFR Part 11 to the Laboratory Environment, Sandy WeinbergThe Good Automated Laboratory Practices, Gerald J. Whartenby, Paul L. Robinson, and Sandy WeinbergImplementing GLP's in a Non-GLP Analytical Laboratory, Stephanie A. OlexaComputer Systems Validation, Sandy WeinbergThe FDA's GLP Inspection Program, George W. JamesThe Future, Sandy Weinberg Bibliography Index
Covers all aspects of the Food and Drug Administration's (FDA), Good Laboratory Practice (GLP) regulations and techniques for implementation. This book details standards and general guidelines for the management of research environment. It examines theoretical principles for anticipating interpretations of GLP in a variety of laboratory settings
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