Eu fmd

GOOD MANUFACTURING PRACTICE (cGMP) REGULATORY TRENDS AND QA
1

Please share some valuable things about EU FMD.

2

Dear,
What would you like to know about FMD? As you may know the FMD guideline will go live from 09 of february 2019. From then each patiënt medication package must have a serialisation number in it and an anti tempering device.
Most manufacturers are very busy at the moment to arrange the last steps before the deadline. Unfortunately there are alot of small problems and discussion points stil,

The MAH’s have to ontboard in the EU hub, etc etc.

Please let me know What you specifically want to know.

Regards

3

Hi,

I want to know each and everything related to EUFMD norms for track and trace. Can you share it?