Aug 11, 2026 - Cosmetics
Frequently Asked Questions about Ph. Eur. Chapter 2.6.12 - EDQM
The EDQM (European Directorate for the Quality of Medicines & Health Care) published some time ago a document containing FAQs on product testing according to Ph. Eur. 2.6.12. This document contains valuable guidance on the correct performance of the microbiological examination and remains valid.
The document essentially covers the following points:
- Preparation, cultivation and propagation of reference strains
- Negative controls
- Growth-promoting properties (Growth Promotion Test)
- Suitability of the test method
- Interpretation of test results
When testing non-sterile medicinal products or medical devices according to the mentioned methodology, it is particularly important that the suitability of the test method be demonstrated in advance. Only in this way can reliable results be achieved.
We carry out this suitability test for you at any time without delay. You will receive the results of this suitability test as well as the results of the examination itself immediately after completion via our online portal myBAV.
Thanks to our many years of expertise in testing a wide range of products and product groups, we can also provide you with comprehensive advice on the results. If microbial growth is observed, we provide rapid identification results using MALDI-TOF technology. Do you have any questions? Call us — we look forward to hearing from you!
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