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Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Pharmaceutical technology

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Pharmaceutical Computer Systems Validation - Quality Assurance, Risk Management and Regulatory Compliance (Hardcover, 2nd edition) Loot Price: R5,574
Discovery Miles 55 740
Pharmaceutical Computer Systems Validation - Quality Assurance, Risk Management and Regulatory Compliance (Hardcover, 2nd...

Pharmaceutical Computer Systems Validation - Quality Assurance, Risk Management and Regulatory Compliance (Hardcover, 2nd edition)

Guy Wingate

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Loot Price R5,574 Discovery Miles 55 740 | Repayment Terms: R522 pm x 12*

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Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements for computer systems, the text extensively reviews regulations of pharmaceuticals, healthcare products, blood processing, medical devices, clinical systems, and biotechnology. Ensuring that organizations transition smoothly to the new system, this guide explains how to implement the new GMP paradigm while maintaining continuity with current practices. In addition, all 24 case studies from the previous edition have been revised to reflect the new system.

Key topics in Pharmaceutical Computer Systems Validation, Second Edition include:

  • GAMP5, ASTM 2500, EU GMP (Annex 11), and US GMP revisions to regulatory requirements for electronic records and signatures that should be published in 2008
  • ICH Guidance Q8, Q9, and Q10 expectations
  • FDA cGMPs for the 21st Century Initiative and associated guidance
  • PIC/S Guidance on Good Practice for Computerized Systems in GxP Environments
  • WK9864 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
  • the indirect developments from FDA/EU/Japan regulators and industry
  • the role of QA department, and internal and external suppliers
  • the integration of computer systems validation into single overall approach for wider system
  • practical guidance on handling common high, medium, and low risk issues that can occur during the life cycle of a computer system
  • managing outsource partners and handling legacy systems
  • topical issues uncovered by regulatory authorities including US FDA

General

Imprint: Crc Press
Country of origin: United States
Release date: February 2010
First published: 2015
Editors: Guy Wingate
Dimensions: 254 x 178 x 46mm (L x W x T)
Format: Hardcover
Pages: 798
Edition: 2nd edition
ISBN-13: 978-1-4200-8894-6
Categories: Books > Science & Mathematics > Biology, life sciences > General
Books > Medicine > General issues > Medical equipment & techniques > Medical laboratory testing & techniques
Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Pharmaceutical technology
LSN: 1-4200-8894-7
Barcode: 9781420088946

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