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.
