april, 2021

22apr2:00 pm4:00 pmIVDR Webinar2:00 pm - 4:00 pm CEST

Event Details

By 26th May 2022, new in-vitro medical devices will have to meet the requirements of the IVDR when sold in the European market.

This is not just a critical business factor but a major roadblock for many companies. To support you best we have partnered with Eurofins Genomicswho have a deep understanding of this situation as many of their customers face the challenge to comply with the new IVD regulation to set up this exclusive IVDR webinar.

Join us on April 22 to this unique (and free) webinar to learn:

✅ Understand key regulatory stakeholders and their expectations
✅ Notified Body – Do’s and don’ts
✅ Technical Documentation – usual methods and best practices
✅ The latest trends in the interpretation of guidance to confirm the right classification and related product families
✅ Applicable standards and regulatory requirements
✅ Documenting the evidence of scientific validity for your IVD (by examples)
✅ And much more!

BONUS: 1h free follow-up consulting by a Medidee Expert for all participants of the live event

Interested in joining us? Follow the link and register!

Time

(Thursday) 2:00 pm - 4:00 pm CEST

Location

Online Event

Organizer

Eurofins Genomics & Medidee

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