News

 

Stay up to date. Use this convenient filter to find the latest news about the medtech sector and Swiss Medtech activities of interest to you.

30.04.25 Press release
Federal Council promotes improved patient care and medtech innovation – Swiss Medtech calls for swift action

Patients in Switzerland should be able to benefit from internationally recognised medical devices. Swiss Medtech welcomes this decision, which will ensure security of supply and support for domestic innovation
30.04.25 News
Federal Council decision on the Müller motion

Federal Council promotes improved patient care and medtech innovation – Swiss Medtech calls for swift action
30.04.25 News
Welcome!

In April, we welcomed two new members to Swiss Medtech.
22.04.25 News
Approve FDA medical devices now!

Ensure supply, promote innovation, strengthen Switzerland as a business location.
10.04.25 News
Innovations at Swiss Medtech Day

Jeroen Tas and Malcolm Werchota present their unique perspectives on the future of medical technology. Their keynotes offer valuable insights into innovation and the challenges facing the industry.
02.04.25 Press release
US tariffs hit medtech industry hard

Flexibility & diversified foreign trade policies increase in importance
01.04.25 News
We are looking for you

The key position of Regulation & Innovation will become vacant at the end of 2025.

20.03.25 News
Responses to the consultation procedures

Our statement on amending the Ordinance on Climate Disclosures has been published.
20.03.25 News
Responses to the consultation procedures

Our statement on KVG amendment on the purchase of funds and objects in the EEA has been published.
12.03.25 News
Swiss Medtech Award 2025: The finalists have been chosen

evismo, QUMEA und Bonebridge have reached the finals for this year’s award
18.02.25 News
Save-the-Date: National Regulatory Conference – 15 October 2025

Themed «Addressing Today’s and Tomorrow’s Pain Points», the regulatory challenges of the Swiss medtech industry will be highlighted.
17.02.25 News
Take part now: Targeted Evaluation of the MDR/IVDR!

The EU Commission is reviewing the MDR and IVDR regulations and needs your feedback! You have until 21 March 2025 to share your experiences.