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European Coalition on Homeopathic & Anthroposophic Medicinal Products

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Regulatory Environment

Chairperson: Dr Astrid Sprenger


This field of activity deals with any developments relating to the construction of a specific and harmonised regulatory environment for homeopathic and anthroposophic medicinal products. ECHAMP monitors regulatory developments such as guidelines and formats for application and quality and safety issues of homeopathic and anthroposophic substances. The group develops models and position papers and comments on proposals published by the competent authorities in consultation with its stakeholders. Active and pro-active contacts with competent authorities are very important for this working party in order to clarify ECHAMP’s points of view. Two permanent Subject Groups currently work under the umbrella of the ECHAMP field of activity "Regulatory Environment”.

Last updated on 16 Sep 2015