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CTO-MedD
SR 810.306 — Ordinance of 1 July 2020 on Clinical Trials with Medical Devices (CTO-MedD).
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:NOTE [links:https://fedlex.data.admin.ch/eli/cc/2020/553]
English is not an official language of the Swiss Confederation. This translation is provided for information purposes only and has no legal force.
English consolidation of 20 May 2025, which is also the date of the current binding text.

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Preamble
The Swiss Federal Council,
based on the Human Research Act of 30 September 2011 (HRA)and on Articles 54 paragraphs 3, 6 and 8, 54b paragraphs 2 and 3 and 82 of the Therapeutic Products Act of 15 December 2000 (TPA),
ordains:
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SR 810.30
SR 812.21

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Contents
1. General Provisions — 6 articles
2. Approval and Notification Procedures — 16 articles
3. ... — 1 article
4. Documentation, Notifications and Reporting — 9 articles
5. Registration and Publication — 2 articles
6. Final Provisions — 10 articles

:LINK
https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2020/553/20250520/en/html/fedlex-data-admin-ch-eli-cc-2020-553-20250520-en-html.html
Official text on Fedlex — consolidation of 20 May 2025