Qualification and validation are two words we use a lot in GMP, and sometimes we interchange them. This blog explains the difference between these two

If you are starting your preparation, aim to be proactive and develop a strategy on how to transition your current CSV framework to a CSA

Do you want to assess whether your organisation is meeting GxP requirements? Use the below checklist and find out whether GxP fundamentals are well-established in

Technical documents, we’ve all seen them, and many of us might have already discovered how deliciously awful they can be. This blog focuses on improving

This article focuses on using the 6M tool as a support of the design of an aseptic isolator. The objective is to provide a generic