Blog

Welcome to the latest news from Metecon! Here we will keep you informed about the latest developments, e.g. regarding our Representative Services EC-REP and CH-REP, exciting projects, and important company and specific branch information.

Discover how we consistently work to support our customers in the areas of Documentation, Regulatory Affairs, Clinical Affairs and Quality Management in the best possible way. A special highlights are our Representative Services EC-REP and CH-REP, where we act as your trusted partner in Europe and Switzerland. Learn more about our customized solutions and how we can help you to meet the regulatory requirements in these markets successfully. Dive into the world of Metecon and stay informed about the latest trends and innovations in the medical device industry.



Regulatory Affairs: Challenges for Swiss manufacturers of medical devices and in vitro diagnostics (IVDs)
August 2023

Regulatory Affairs: Challenges for Swiss manufacturers of medical devices and in vitro diagnostics (IVDs)

Challenges for Swiss manufacturers of medical devices and in vitro diagnostics in the area of Regulatory Affairs and New MDR and IVDR transition periods
IvDO - Regulation of In vitro diagnostics (IVDs) in Switzerland
July 2023

IvDO - Regulation of In vitro diagnostics (IVDs) in Switzerland

Learn about the regulation of in vitro diagnostics (IVD) in Switzerland according to the latest legal provisions.
Are we meeting at Swiss Medtech Day?
June 2023

Are we meeting at Swiss Medtech Day?

Discover the regulatory compliance services of Metecon Switzerland GmbH at the Swiss Medtech Day in Bern and find out how we support medical technology companies!