EDQM

The EDQM, part of the Council of Europe, plays a central role in harmonizing and promoting the quality of medicines and healthcare across its 46 member states and beyond. Founded in 1964, the EDQM is responsible for developing and maintaining the European Pharmacopoeia (Ph. Eur.), which sets legally binding quality standards for pharmaceutical substances and products throughout Europe.

In addition to pharmacopoeial work, EDQM also oversees certification procedures (CEP – Certificate of Suitability), the coordination of Official Medicines Control Laboratories (OMCLs), and activities related to blood transfusion, organ transplantation, and consumer health protection. These initiatives support public health by ensuring the safety, efficacy, and quality of medicinal products available in the market.

EDQM’s scientific rigor and regulatory authority make it a cornerstone of pharmaceutical quality assurance not only in Europe but globally. Its standards are used by manufacturers, regulators, and quality control labs to ensure compliance and enhance patient safety across the entire pharmaceutical supply chain.