Regulations for clinical trials of medical devices
Switzerland has adapted its medical devices regulations to the EU rules in the interests of patient safety and EU market access for the Swiss medical devices industry. The changes also have implications for human research legislation.
Federal Office of Public Health FOPH
Biomedicine Division
Human Research Section
Schwarzenburgstrasse 157
Switzerland - 3003 Bern
Human Research Section
Schwarzenburgstrasse 157
Switzerland - 3003 Bern