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Tag: ClinO-MD
ClinO-MD: The Swiss regulatory framework guiding clinical trials with medical devices.
The Importance of a Monitoring Plan in MR Medical Device Studies
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Revision of Human Research in Switzerland — The Revised HRA Ordinances
Switzerland has taken a significant step forward in regulating human research with the revision of the Human Research Act (HRA) ordinances. Approved by the Federal Council, the updated ordinances, designed to reflect advancements in digitalization, national and international standards, and research practices, officially came into effect on 1 November 2024. However, provisions on transparency will… Continue reading Revision of Human Research in Switzerland — The Revised HRA Ordinances
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