Loading
BAYOOSOFT
  • Management Solutions
    • IT-Security
      • Access Manager
      • gpg4o
    • MedTech
      • Reinventing Technical Documentation
      • Risk Manager
      • MEDiLEX
    • Telesolutions
      • HospiX
  • About us
    • BAYOOSOFT
      • Software Made in Germany
      • The Co-thinker Team
      • Contact Us
    • News & Events
      • News
      • Events
    • BAYOONET Group
      • BAYOOTEC
      • BAYOOMED
  • Jobs & Career
  • Shop
  • Search
  • Menu

Consequences for the medtech industry

No agreement between Switzerland and the EU

It has burst. The new agreement between Switzerland and the EU will not enter into force. After seven years of negotiations between representatives of the EU Commission and Switzerland, President Guy Parmelin declared the talks a failure yesterday. The reason, he said, was disagreement on crucial points of the negotiations, such as access to the EU’s internal market and agreements on the free movement of persons. The modernisation of the agreement, which has been in place since 1972, has thus failed to materialise.

A failure that particularly affects the Swiss medtech sector shortly after the transition to the new MDR 2017/745. What does this mean for access to the EU internal market?

Due to the loss of privileged access, Switzerland will now be downgraded to the status of a third country. Manufacturers must therefore adapt when placing new medical devices on the European market.

The consequences are additional work due to increased requirements and having to go through the European approval process. In addition to the designation of a specific Notified Body, the preparation of corresponding technical documentation is also required.

As a Swiss company, are you affected by the collapsed framework agreement?

Contact us. We have developed a system with which you can create a CE-compliant variant from your existing technical documentation. With the help of the validated software solution, you can implement this independently and make a new product file for a class IIb medical device ready for documentation within six weeks. Guaranteed – because we assure you of the compliance of the technical documentation.

In this way, you efficiently accelerate the approval of your medical device despite the new situation.

Do you have a question? Contact us!

We look forward to hearing from you.

Our Succes Story

How we were able to help MST-Instrumente GmbH save labour and time in processing according to IEC 60601-1? Read more about our shared history here:

Would you like to get to know the validated approval accelerator directly free of charge? Sign up for a 30-day TRIAL.

Test now for free

Latest News

  • BAYOOSOFT @ MEDICA 202231. October 2022 - 19:09
  • Ein:e Ärtz:in sitzt vor einem Tablet und hat ein Stethoskop um den HalsClinical evaluation according to MDR5. October 2022 - 14:31
  • Header Bild, Bildschirm mit Schloss-SymbolEmail encryption – Which method is the most secure?13. May 2022 - 14:23
Contacts at BAYOOSOFT 

Svenja Winkler
CEO
[email protected]

 

 

Franziska Weiß
Head of Sales
[email protected]

Darmstadt
Lise-Meitner-Straße 10
64293 Darmstadt

Munich
Aidenbachstraße 54
81379 München

Berlin 
Mariendorfer Damm 1-3
12099 Berlin

Contact: [email protected]bayoosoft.com
Jobs: [email protected]
Press: [email protected]

Phone: +49 (0) 6151 – 86 18 – 0
Fax: +49 (0) 6151 – 86 18 – 150

Contact support
  • Privacy Policy
  • Legal
BAYOOSOFT @DMEA 2021 Sabotage protection – or how to double-secure internal company secret...
Scroll to top