Ce programme a été conçu pour permettre aux participants de développer leurs connaissances et de se familiariser avec les travaux et procédures de la Pharmacopée Européenne dans le domaine des médicaments homéopathiques.
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Public concerné
Cette formation intéressera particulièrement les autorités réglementaires nationales, les fabricants et les managers chargés du contrôle qualité ou des affaires réglementaires dans le domaine des médicaments homéopathiques.
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- European regulations for medicines: Place and role of the EDQM and the European Pharmacopoeia by Cathie Vielle
- General concepts in the European Pharmacopoeia: theory and rationale | How to find your way in the Ph. Eur. General Notices, General Chapters, General monographs by Dr Emmanuelle Charton
- Structure of the European Pharmacopoeia by Catherine Lang
- Overview on requirements for homoeopathic products of chemical origin: A guide through the different sections by Catherine Lang
- Overview on requirements for homoeopathic products of herbal origin: A guide through the different sections by Catherine Lang
- Homoeopathic monograph case study by Prof. Michael Keusgen
- Overview on requirements for dosage forms and manufacturing methods of homoeopathic medicinal products by Dr Julia Maier
- European Pharmacopoeia Reference Standards: Overview of the policy and process used to establish and distribute a reference standard by Dr Matthias Weber
- How to participate in the elaboration of the European Pharmacopoeia by Dr Julia Maier
- How to make the best use of EDQM website, Pharmeuropa website, Knowledge database by Dr Hans-Joachim Bigalke
Download the presentations
- European regulations for medicines: Place and role of the EDQM and the European Pharmacopoeia by Cathie Vielle
- General concepts in the European Pharmacopoeia: theory and rationale | How to find your way in the Ph. Eur. General Notices, General Chapters, General monographs by Dr Emmanuelle Charton
- Structure of the European Pharmacopoeia by Catherine Lang
- Overview on requirements for homoeopathic products of chemical origin: A guide through the different sections by Catherine Lang
- Overview on requirements for homoeopathic products of herbal origin: A guide through the different sections by Catherine Lang
- Homoeopathic monograph case study by Prof. Michael Keusgen
- Overview on requirements for dosage forms and manufacturing methods of homoeopathic medicinal products by Dr Julia Maier
- European Pharmacopoeia Reference Standards: Overview of the policy and process used to establish and distribute a reference standard by Dr Matthias Weber
- How to participate in the elaboration of the European Pharmacopoeia by Dr Julia Maier
- How to make the best use of EDQM website, Pharmeuropa website, Knowledge database by Dr Hans-Joachim Bigalke
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