Specific topics include the role of pharmaceutical reference standards during the pharmaceutical lifecycle, the role of compendial reference standards and regulatory perspectives on impurities standards.
The programme has been designed to give participants a greater insight into the work and procedures of the European Pharmacopoeia (Ph. Eur.) and related activities of the EDQM.
HYBRID - EDQM PREMISES, STRASBOURG, FRANCE & ONLINE
This training programme takes a closer look at the principles and procedures underpinning the Official Control Authority Batch Release (OCABR) for Human Vaccines in the EU/EEA.