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October 13, 2016
The European Medicines Agency (EMA) has started a public consultation on its draft revision of the scientific guideline on the assessment of clinical safety and efficacy in the preparation of European Union herbal monographs for well-established and traditional herbal medicines.
The changes aim to provide updates based on advances over the last 10 years and to adopt the latest established practices and legal interpretations.
Comments may be submitted until November 30, 2016.
