
Representation and support for manufacturers in the healthcare, beauty, and other industries.
We support your products’ launch to the Swiss market through documentation review and product registration.

Since 26 May 2021, manufacturers of class I medical devices must comply with the Swiss…

Latest changes in the EU: how the new transitional provisions impact the Swiss Medical Devices Ordinance
The initial transition periods foreseen by the Medical Devices Regulation (MDR) for legacy devices were…

Swiss requirements for combination products
The lack of a renewed Mutual Recognition Agreement (MRA) on the medical device legislation between…