Facility Validation

Often considered a necessary evil by the pharmaceutical industry validation is still understood by many as unrestrained bureaucracy paperwork and procedures whose roots and logic are obscure and only serve to slow down progress. Thoroughly defining the philosophy application and processes Facility Validation: Theory Practice and Tools explores the validation issues relevant to the start-up of a new or upgraded manufacturing facility.The author describes policies guidelines and regulations relating to GMPs in the pharmaceutical industry and explores the relationship between these GMPs and the validation process. He outlines the theory and clarifies the philosophy and key principles of validation such as life-cycle approach and qualification practices. The book includes coverage of common pitfalls and how to avoid them the difficulties and constraints a validation team has to manage and the dangers of not adopting and following the recommended best practices.Facility validation has in fact become good business. It can be a tool for enhancing reliability cost and quality. This book makes the case that design engineering commissioning and validation activities can be integrated and streamlined to accelerate a pharmaceutical manufacturing plant start-up effort and demonstrates how to use best practices to achieve the results you desire in your organization.