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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.

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

Register here! 
 

SDS MedteQ
Svärdvägen 23
182 33 Danderyd
Danderyds kommun
Sverige
VAT nummer: SE5568945231

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