The EDQM is ISO 9001:2015 certified for the following activities:
• Evaluation of applications for certificates of suitability to the monographs of the European Pharmacopoeia and management of the inspection programme of manufacturing sites and associated brokers”.;
• Planning, implementation and coordination of post-marketing surveillance studies for medicinal products and management of related databases;
• Coordination of the elaboration and issuance of guidelines related to the OCABR procedure for the release of batches of human immunological medicinal products (blood and vaccines);
• Management of the elaboration, revision, correction and suppression of European Pharmacopoeia texts, their publication in printed and electronic format and their distribution;
• Conduct of laboratory studies.