Good laboratory practice regulations / edited by Sandy Weinberg.
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TextLanguage: English Series: Drugs and the pharmaceutical sciences ; v. 124Publication details: New York : Marcel Dekker, 2003. Edition: 3rd edDescription: x, 244 p. ; 23 cmISBN: 0824708911 (alk. paper); 9780824708917Subject(s): Medical laboratories -- Quality control | Pharmaceutical technologyDDC classification: 615.19 LOC classification: R850 | .G66 2003Online resources: Publisher description | E-book Fulltext | Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds |
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| 615.19 COM 2004 Computational medicinal chemistry for drug discovery / | 615.19 DRU 2005 Drug discovery handbook / | 615.19 FOF 2013 Foye's principles of medicinal chemistry / | 615.19 GOO 2003 Good laboratory practice regulations / | 615.19 GRI 1997 Introduction to medicinal chemistry : | 615.19 HAN 2000 Handbook of microbiological quality control : | 615.19 HAN 2003 Handbook of isolation and characterization of impurities in pharmaceuticals / |
Includes bibliographical references (p. 229-237) and index.
TOC 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 WeinbergBibliographyIndex
Summary:
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
Pharmacy
Sagar Shahanawaz
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