Compressed air systems are a critical component of many pharmaceutical manufacturing facilities. With any new system creation, addition, or change, a validation should be performed to ensure the ...

Compressed air is often overlooked as a potential source of clean room and product contamination. This webinar will give you an understanding of the different types of contamination inherent in ...

To qualify and validate a pharmaceutical manufacturing facility, one must carefully review the facility design for compliance with good manufacturing practices and manage project scope definition, ...

It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the ...

It's no longer news that the growing emphasis on sustainability is leading the charge for higher efficiency. When discussing energy use in manufacturing environments, the Big Three - water, ...