Innehållet nedan modereras inte i förväg och omfattas därmed inte av webbplatsens utgivningsbevis.
Dela sida
Sponsrat innehåll

Webinar: Medtech quality and regulatory compliance

This webinar is for you who are developing or planning to develop a medical device, combination, or borderline product. In one hour, we will discuss what you need to pay extra attention to, pitfalls, and what you shouldn’t forget going forward.

Register HERE!


  • What counts as a medical device/IVD.
  • How to pick the right regulatory strategy with your business lens.
  • The importance of sharpening claims to gather appropriate clinical data.
  • Identifying the right expertise for your product.
  • Must-do’s during product development.

The presenters will be Anna-Karin Alm, Managing Director of SDS MedteQ and Farha Sayeed, Regulatory Affairs Consultant.

Cytel Sweden
Sankt Eriksgatan 113, 3 tr
113 43 Stockholm
Stockholms stad
VAT nummer: SE7104093021


Sänd till en kollega