- Annex 1 revision (SYD-01-03-18)
9:00 am - 4:00 pm
The European Medicines Agency (EMA) has published the public draft of the long-awaited revision to Annex 1 of their GMPs, for the Manufacture Sterile Medicinal Products.
This training course will dive deeper into the revisions and highlight changes that need to be considered for sterile manufacturers with markets subject to EMA or PIC/S.
You may be required to comply quickly with these new changes, so come along to this training session and hear from the experts who have been following the changes closely over the last couple of years.