Read Good Laboratory Practice for Nonclinical Studies

Good Laboratory Practice for Nonclinical Studies

Graham P Bunn

4.9/5 (32708 ratings)

Description:The GLP regulations have been enacted since 1978 and are currently under a proposed FDA amendment to revise terminology and accommodate other changes relating to advances in technology related to the industry. This book provides a unique opportunity to access interpretation of the 21CFR58 regulatory requirements from leading industry experts with a vast knowledge and expertise in their fields. The approach used takes the regulations, provides interpretations and references to examples and regulatory actions. Data integrity and the use of electronic systems in compliance with 21CFR11 Electronic Records: Electronic Signatures are also discussed.- Unique volume covering FDA inspections of GLP facilities- Provides a detailed interpretation of GLP Regulations- Presents the latest on electronic data management in GLP- Describes GLP and computer systems validation- Can be referenced repeatedly in supporting daily hands on implementation of the CFR requirementsWe have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Good Laboratory Practice for Nonclinical Studies. To get started finding Good Laboratory Practice for Nonclinical Studies, you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

Pages: 194

Format: PDF, EPUB & Kindle Edition

Publisher: CRC Press

Release: 2022

ISBN: 1000789578

Description: The GLP regulations have been enacted since 1978 and are currently under a proposed FDA amendment to revise terminology and accommodate other changes relating to advances in technology related to the industry. This book provides a unique opportunity to access interpretation of the 21CFR58 regulatory requirements from leading industry experts with a vast knowledge and expertise in their fields. The approach used takes the regulations, provides interpretations and references to examples and regulatory actions. Data integrity and the use of electronic systems in compliance with 21CFR11 Electronic Records: Electronic Signatures are also discussed.- Unique volume covering FDA inspections of GLP facilities- Provides a detailed interpretation of GLP Regulations- Presents the latest on electronic data management in GLP- Describes GLP and computer systems validation- Can be referenced repeatedly in supporting daily hands on implementation of the CFR requirementsWe have made it easy for you to find a PDF Ebooks without any digging. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Good Laboratory Practice for Nonclinical Studies. To get started finding Good Laboratory Practice for Nonclinical Studies, you are right to find our website which has a comprehensive collection of manuals listed.
Our library is the biggest of these that have literally hundreds of thousands of different products represented.

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Good Laboratory Practice for Nonclinical Studies

Good Laboratory Practice for Nonclinical Studies

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