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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!

Content

  • 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
Sverige
VAT nummer: SE7104093021

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