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Good laboratory practice regulations / edited by Sandy Weinberg.

Contributor(s): Weinberg, Sandy, 1950-Material type: TextTextLanguage: 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
Contents:
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: 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
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Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
E-Book E-Book Dr. S. R. Lasker Library, EWU
E-book 		Non-fiction 615.19 GOO 2003 (Browse shelf(Opens below)) Not for loan
Text Text Dr. S. R. Lasker Library, EWU
Reserve Section 		Non-fiction 615.19 GOO 2003 (Browse shelf(Opens below)) C-1 Not For Loan 17294
Text Text Dr. S. R. Lasker Library, EWU
Reserve Section 		Non-fiction 615.19 GOO 2003 (Browse shelf(Opens below)) C-2 Not For Loan 17326
Text Text Dr. S. R. Lasker Library, EWU
Circulation Section 		Non-fiction 615.19 GOO 2003 (Browse shelf(Opens below)) C-3 Available 18589
Total holds: 0

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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