Good laboratory practice regulations [electronic book] / edited by Sandy Weinberg.
Contributor(s): Weinberg, Sandy
.
Material type: 
BookSeries: Drugs and the pharmaceutical sciences: Publisher: New York : Informa Healthcare, c2007Edition: 4th edition.Description: online resource (vii, 285 pages).Content type: text Media type: computer Carrier type: online resourceISBN: 9780849375835 (hardback); 9780849375842 (e-book).Subject(s): Medical laboratories -- Quality control | Medical laboratories -- Law and legislation | Biological laboratories -- Quality control | Pharmaceutical technologyGenre/Form: Electronic booksAdditional physical formats: Print version:.: Good laboratory practice regulations.DDC classification: 615.19072 Online resources: Access eBook Also available in print form.
| Item type | Current library | Call number | Status | |
|---|---|---|---|---|
| eBook | MTU Online eBook | 615.19072 (Browse shelf(Opens below)) | Available |
Enhanced descriptions from Syndetics:
Recent changes in the interpretation and enforcement of 21 CFR Part 11 have shifted the focus of Good Laboratory Practice (GLP) regulations to concentrate on the acceptance of electronic signatures, the archiving of data, the security of electronic documents, and the automation of laboratory procedures. This all-encompassing Fourth Edition addresses every critical aspect of Good Laboratory Practice (GLP) regulations and demonstrates effective strategies for implementation in a variety of laboratory settings. This updated and expanded classic text contains new information about applying 21 CFR Part 11 to the laboratory environment, GLP documentation systems, laboratory risk analysis, system validation and inspection, process analytical technologies, and cost control for the prevention of pitfalls and the assurance of compliance in numerous research environments.
Providing insights for the application of GLP regulations and emphasizing the latest regulatory developments, this reference discusses the implementation of PAT and emphasizes the importance of electronic audit trails and data controls as laboratories rely more on automated procedures...gives clear rules for the acceptance of electronic signatures, archiving of data in formats accessible by electronic recovery and human retrieval, and the security of electronic documents...and details the FDA's GLP inspection program.
Includes bibliographical references and index.
CIT Module CHEM 8003 - Core reading
Also available in print form.
Electronic reproduction.: ProQuest LibCentral. Mode of access: World Wide Web.
Table of contents provided by Syndetics
- Preface (p. iii)
- Contributors (p. vii)
- 1 Historical Perspective (p. 1)
- 2 FDA/GLP Regulations (p. 25)
- 3 Regulation of Computer Systems (p. 111)
- 4 The Good Automated Laboratory Practices (p. 131)
- 5 Implementing GLPs in a Non-GLP Analytical Laboratory (p. 151)
- 6 Controlling the Good Laboratory Practices Inspection Process (p. 167)
- 7 Computer Systems Validation (p. 193)
- 8 GLP Documentation (p. 223)
- 9 The FDA's GLP Inspection Program (p. 241)
- 10 The Future of the Good Laboratory Practice Regulations (p. 259)
- Index (p. 271)