Good Laboratory Practice Regulations

✍ Scribed by Sandy Weinberg

Publisher: CRC Press
Year: 2007
Tongue: English
Leaves: 295
Series: Drugs and the Pharmaceutical Sciences
Edition: 4th Edition
Category: Library

No coin nor oath required. For personal study only.

✦ Synopsis

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.

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