0
Your cart

Your cart is empty

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

Buy Now

Pharmaceutical Computer Systems Validation - Quality Assurance, Risk Management and Regulatory Compliance (Hardcover, 2nd edition) Loot Price: R5,563
Discovery Miles 55 630
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

 (sign in to rate)
Loot Price R5,563 Discovery Miles 55 630 | Repayment Terms: R521 pm x 12*

Bookmark and Share

Expected to ship within 10 - 15 working days

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
Promotions
LSN: 1-4200-8894-7
Barcode: 9781420088946

Is the information for this product incomplete, wrong or inappropriate? Let us know about it.

Does this product have an incorrect or missing image? Send us a new image.

Is this product missing categories? Add more categories.

Review This Product

No reviews yet - be the first to create one!

You might also like..

Practical Aspects of Vaccine Development
Parag Kolhe, Satoshi Ohtake Paperback R3,975 Discovery Miles 39 750
Modern Approaches in Drug Discovery…
Charles Lesburg Hardcover R4,309 Discovery Miles 43 090
Drug Delivery Nanosystems for Biomedical…
Chandra P Sharma Hardcover R3,811 R3,555 Discovery Miles 35 550
Quantitative Systems Pharmacology…
Davide Manca Hardcover R5,419 R5,013 Discovery Miles 50 130
Handbook of Cosmeceutical Excipients and…
Y H Kwan, Y K Tung, … Hardcover R3,770 Discovery Miles 37 700
Therapeutic Risk Management of Medicines
Stephen J. Mayall, Anjan Swapu Banerjee Hardcover R4,565 Discovery Miles 45 650
Orphan Drugs - Understanding the Rare…
Elizabeth Hernberg-Stahl, Miroslav Reljanović Hardcover R4,210 Discovery Miles 42 100
Lean Biomanufacturing - Creating Value…
Nigel J. Smart Hardcover R4,223 Discovery Miles 42 230
Formulation Tools for Pharmaceutical…
J. E. Aguilar Hardcover R3,792 Discovery Miles 37 920
Computer-Aided Applications in…
Jelena Duris Hardcover R3,335 Discovery Miles 33 350
Therapeutic Protein Drug Products…
Brian K. Meyer Hardcover R3,436 Discovery Miles 34 360
Intelligent Materials for Controlled…
Steven M Dinh, John DeNuzzio, … Hardcover R2,327 Discovery Miles 23 270

See more

Partners