2 December 2022
Public consultation on ICH Guideline M11 “Clinical electronic Structured Harmonised Protocol (CeSHarP)” launched in Switzerland
Swissmedic launches the public consultation on Guideline M11 of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH Guidelines), with a deadline of 26 February 2023 for comments.
For more information, see here.
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Swissmedic: New strategic Approach to minimizing Animal Testing in the Development of Medicinal Products
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Swissmedic: The new Pharmacopoea Helvetica 13
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European Medicines Agency: New oral GLP-1 Medicine for Weight Management and Type 2 Diabetes
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FOPH: Capital Income of Health Insurers for Premium Reduction – current voluntary System deemed sufficient
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Swissmedic: Haemovigilance Annual Report 2025
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Decision C-6534/2024 of 13 October 2026
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Swissmedic: GMP Compliance by foreign Manufacturers - Simplifications for Industry and Clarification of unresolved Issues
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European Medicines Agency: Clinical Trial Applications Advice Pilot becomes permanent
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Swissmedic: Revision of the Guidance document Authorisation Biosimilar