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- 2014
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- 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"
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- Pyrogenicity: Commission strategy for removing or replacing the rabbit pyrogen test
- Examples of implementation of pharmacopoeial procedures according to Chapter 5.26 "Implementation of pharmacopoeial procedures”
- 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
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