In the world of Good Manufacturing Practice (GMP), complete documentation is indispensable, especially for the qualification and validation of software. It is the proof of conformity and safety of your processes. However, as system complexity grows, the volume of documents can easily explode, jeopardizing clarity.
To make the qualification process as simple and efficient as possible for you, we have fundamentally revised our entire lifecycle documentation. We have introduced a new hierarchy and structure that:
With this new structure, you maintain an overview at all times and minimize the administrative effort of your validation projects.