This thoroughly authoritative work furnishes organizational, technological, validation, project management, and business perspectives on pharmaceutical information automation from industry and system automation professionals-demonstrating how to fulfill computer system validation requirements for hardware, applications, networks, data center operations, and complex software management practices in pharmaceutical manufacturing.
Explains how the Food and Drug Administration’s latest Good Manufacturing Process guidelines supporting electronic identification and electronic signatures for batch record registration together with computer system technologies will influence pharmaceutical production automation!
Designed to provide quick and easy access to a whole range of system development topics, Automation and Validation of Information in Pharmaceutical Processing

defines a complete life-cycle methodology that integrates equipment, people, and information

presents concepts, guidelines, test plans, example forms, and application details for previously unavailable computer system validation of complex automated information systems

introduces, for the first time in depth, PQ testing of integrated manufacturing execution (MES) and manufacturing resource planning (MRP) applications

describes how human resource programs maximize productivity gains for automation initiatives

discusses approaches to automating batch operations with process control systems using industry examples and applicable computer technology concepts

provides an outline for IQ, OQ, and PQ test plans for process control systems, including forms for use in testing instrumentation and distributed control system installation and operations

employs a business analysis standpoint on life-cycle planning to justify new automation projects, including multiyeardrug manufacturing plans

documents the successful app

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