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.
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.
