The European Directorate for the Quality of Medicines (EDQM) emerged from the European Medicines Commission in 1994. The EDQM is responsible for the publication of the European Pharmacopoeia, the issuing of CEP certificates, as well as the characterisation and dispatch of reference substances. The EDQM is also the headquarters of the OMCL network for the quality control of human and veterinary medicinal products.
[GMP Compliance Adviser, Chapter B.2]
You can find out more about this topic:
The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business!