Webinar: Medtech quality and regulatory compliance – the basics!

This webinar is for you 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.