- Noname
- Noname
- ----
- Noname
- Draft harmonised texts for comment
- No draft texts currently for comment
- Pharmacopoeial harmonisation
- Partners in pharmacopoeial harmonisation
- Pharmeuropa Bio & Scientific Notes and Readers' Tribune
- 2014
- 2013
- 2012
- 2011
- Re-examination of the general monographs on Herbal drugs and Herbal drug preparations with reference to monographs on traditional Chinese herbal ingredients
- Comments on the article of Dr Keith Helliwell on European Pharmacopoeia monographs on extracts
- Heparins and changing regulatory requirements in the EU
- 2010
- Nanopharmaceuticals: implications for the European Pharmacopoeia
- European Pharmacopoeia monographs on extracts: reflections following recent discussions
- System suitability criteria and variation of parameters in capillary zone electrophoresis
- Ph. Eur. / USP prospective harmonisation – API pilot project: industry perspective
- Comments on "European Pharmacopoeia monographs on extracts: reflections following recent discussions"
- noname
- Extractable elements in plastic materials for pharmaceutical use (2.4.35.)
- Veterinary vaccines: update of the approach to extraneous agent testing in IVMPs (implementation date 1st July 2020) - What has changed and why
- Ph. Eur. Section 3. Materials for containers: clarification of legal status
- Examples of validation protocols of the alternative microbiological methods according to chapter 5.1.6 Alternative methods for control of microbiological quality
- Reverse osmosis in Ph. Eur. monograph Water for injections (0169)
- Bacterial endotoxins: European Pharmacopoeia policy (revised February 2015)
- Response and correction factors in monographs of the European Pharmacopoeia
- Homoeopathic preparations: changes to titles of monographs
- Veterinary vaccines: harmonisation with VICH Guidelines 41 and 44
- 10th Edition
- Publication schedule and general information (December 2021)
- Comments concerning revised texts published in Supplement 10.8
- List of texts published in Supplement 10.8
- Texts adopted by the Commission in November 2021
- Comments concerning revised texts published in Supplement 10.7
- List of texts published in Supplement 10.7
- New reagents added in the European Pharmacopoeia (Supplement 10.7 included)
- Reagents deleted from the European Pharmacopoeia
- Texts adopted by the Commission in June 2021
- Texts adopted by the Commission in March 2021
- Comments concerning revised texts published in Supplement 10.6
- List of texts published in Supplement 10.6
- New reagents added in the European Pharmacopoeia (Supplement 10.6 included)
- Introduction (chapter II) of the 10th Edition (10.0)
- Work of the European Pharmacopoeia
- Pharmeuropa Bio & Scientific Notes and Readers' Tribune
- noname
- HelpDesk and FAQs
- Free EDQM databases
- Certification of suitability to the monographs of the European Pharmacopoeia
- Proficiency Testing Scheme (PTS)
- CombiStats: a statistical tool for the analysis of biological data
- Structure of EDQM
- Membership and observership of the European Pharmacopoeia Commission
- EDQM
- European Pharmacopoeia 10th Edition
- Standard terms
- European Pharmacopoeia reference standards
- European Paediatric Formulary
- Cosmetics and consumer health
- Blood transfusion guides
- Organ, tissue and cell transplantation guides
- Pharmaceuticals and pharmaceutical care
- Counterfeit medical products and similar crimes
- Proceedings of international conferences
- Ph. Eur. Technical guides
- Council of Europe