Critical Gaps - Developing And Optimizing Cleaning Processes

Cleaning validation can be among the most painful and time-intensive aspects of cGMP manufacturing for pharmaceutical, biotech and medical device manufacturers.  Register to download this new whitepaper to...

- Learn some best practices for an optimized cleaning validation process 

- Understand why thorough development, prior to validation, is so critical to the success of your cleaning validation process.

- Get a list of the steps involved in developing a cleaning validation process and key considerations.

- Read a real-world example of how Azzur Group helped a client optimize their cleaning validation process to be more efficient -- developing a process that takes less time, uses less water and cleaning resources and is less complex for staff -- all while maintaining their compliance and risk.

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