The pharmaceutical cleanroom with media infrastructure is not a GMP clean room after completion and commissioning.
The successful transition begins early in the project phase, together with the qualification team.
For building technology, the procedure according to the VDI 6039 guidelines can be a possible variant. The successful completion of mechanical construction and commissioning comletition provides the basis for successful qualification phases.
Collaboration and careful execution of the qualification phases, a successful transition to a GMP clean room can be guaranteed.
It is essential that all parties work towards the same goal.