Webinar | Medtech quality and regulatory compliance

March 16th, 8:30-9:30 CET

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.

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When you've registered, you will get an email with your invitation and link to the webinar.

We will record the webinar. By attending, you agree that your name can be shown in the recording.

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Webinar: What is regulatory affairs?

This webinar is intended for those who work within the life science sector and would like to gain a general understanding of regulatory affairs for human medicinal products. Erika Spens will guide you through regulatory affairs during development, market authorization application, and life cycle management.

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Webinar: Medtech quality and regulatory compliance – the basics!

March 16th, 8:30-9:30 CET

Content:

Check out our other webinars below 👇

Webinar: What is regulatory affairs?

Send your inquiry below

Webinar: Medtech quality and regulatory compliance – the basics!

March 16th, 8:30-9:30 CET

Content:

Check out our other webinars below 👇

Webinar: What is regulatory affairs?

Send your inquiry below

SDS has joined Cytel