White Paper — Sponsored Content

Critical Gaps: Developing and Optimizing Cleaning Processes

Critical Gaps: Developing and Optimizing Cleaning Processes

Cleaning validation can be among the most painful and time-consuming aspects of GMP manufacturing for pharmaceutical developers, but "more complex" does not always mean "more compliant". In this new whitepaper, the Azzur Group's head of Cleaning Validation Services explains best practices for an optimized cleaning validation process and why thorough development, prior to validation, is so critical to success. It shares steps involved in developing a cleaning validation process and a real-world example of how a manufacturer optimized their cleaning validation process to be more efficient while maintaining their compliance and risk.

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