Author:
Edition: 2
Binding: Hardcover
ISBN: 1420088947
Edition: 2
Binding: Hardcover
ISBN: 1420088947
Pharmaceutical Computer Systems Validation: Quality Assurance, Risk Management and Regulatory Compliance
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. Pharmaceutical Computer Systems Validation : Quality Assurance, Risk Management and Regulatory Compliance, Second Edition, ISBN-13: 9781420088946, ISBN-10: 1420088947 Read medical textbooks online like Pharmaceutical Computer Systems Validation here
Pharmaceutical Computer Systems Validation: Quality, Assurance, Risk Managem
Store Search search Title, ISBN and Author Pharmaceutical Computer Systems Validation: Quality, Assurance, Risk Management and Regulatory Compliance by Wingate Estimated delivery 4-14 business days Format Hardcover Condition Brand New Rev. ed. of: Computer systems validation / editor, Guy Wingate. Boca Raton, Fla.: Interpharm/CRC, c2004. Publisher Description Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validati
Categories: Pharmaceutical industry->Standards, Software Validation. Contributors: Guy Wingate - Editor. Format: Hardcover
Categories: Pharmaceutical industry->Standards, Software Validation. Contributors: Guy Wingate - Editor. Format: Hardcover
"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
Pharmaceutical Computer Systems Validation Online
