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Brown glass vials and ampoules containing primary reference standards from the European Pharmacopoeia. The caps are blue with EDQM in gold print and the labels are white, blue and yellow.
Brown glass vials and ampoules containing primary reference standards from the European Pharmacopoeia. The caps are blue with EDQM in gold print and the labels are white, blue and yellow.

Ph. Eur. Reference Standards

European Pharmacopoeia RSs help you produce high quality medicines compliant with EU Standards

Official Ph. Eur. Reference Standards are required to verify compliance with the legal requirements of the European Pharmacopoeia. More than 3000 RS are available, developed with the technical expertise of the EDQM: ISO 9001 certified and ISO 17025 accredited.

With EP primary RSs, you’ll be able to verify your compliance with the official quality standards of the EU, enabling you to access markets everywhere the standards of the European Pharmacopoeia are required or accepted. And as a Labmix24 customer, you also gain access to our excellent, personal customer and scientific support.

We offer the following products and services:

Explore our range of European Pharmacopoeia standards:

Need support finding Ph. Eur. or WHO reference standards? Call or e-mail us today:  +49 2852 96064 00 or info@labmix24.com

About the European Pharmacopoeia

The European Pharmacopoeia (Ph. Eur.) is a reference work for the quality control of human and veterinary medicines throughout their life cycles. It contains the official quality standards that are legally binding in 39 European countries and applied in over 120 countries worldwide.

The current 11th Edition of the Ph. Eur. contains over 3000 texts (monographs) describing quality standards for substances used in the manufacture of medicines or ingredients in medicines, such as active pharmaceutical ingredients (APIs), excipients, herbal ingredients, etc. for finished products, for classes of substances, and for analytical methods. Crucially for quality control, it also addresses the issue of impurities at every stage and from every possible source in the manufacture of medicine.