17 February 2025
Swissmedic: Assessment of post-market surveillance documentation
Swissmedic conducted an assessment to determine the compliance with post-market surveillance requirements for 30 legacy medical devices in risk classes IIa and higher.
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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Decision C-6534/2024 of 13 October 2026
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Swissmedic: Haemovigilance Annual Report 2025
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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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European Medicines Agency: Global regulators call for advancing alternatives to animal testing