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
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