Don’t miss this unique opportunity to learn suggested strategies and best practices that lead to successful IVDR transition and outcomes!

Don’t miss this unique opportunity to learn suggested strategies and best practices that lead to successful IVDR transition and outcomes!
In November 2021, ADCO MED published an information document on Directive 2019/90/EU. The document collects answers on various topics discussed by the Member States market surveillance authorities and the European Commission. We summarize it in this article!
We met with over 400 manufacturers from more than 50 countries in MEDICA’s halls. Here are the latest news and insights we got from medical manufacturers.
Medical device trade is affected by MDR and lack of MRA update. Find out all the details!
Read on the Swiss Federal Council unsigned Institutional Framework Agreement (InstA).
Many changes are occurring on the European continent concerning transport, import and distribution. The main reasons are the consequences of Brexit and the new Medical Device Regulation, that will become fully applicable on the 26th of May 2021.
On November 3rd, 2020, Obelis and QUNIQUE announced a strategic partnership to exchange expertise and knowledge in the field of the MDR & IVDR
With MDR quickly approaching, the Swiss Medtech urges for solution to eliminate technical barriers to trade medical devices in the EU. Read more here!
Learn more about the new procedures for medical device procurement in Vietnamese public health facilities and free sales certificate requirements and limits.
Swiss MDR Deadline has passed! Appoint a Swiss Authorized Representative now! Get in touch