4 November 2022
COVID-19 vaccines: authorised
The European Commission authorised the conversion of the conditional marketing authorisation for Vaxzevria to standard marketing authorization.
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