Webinar on Transitioning to the new EU IVD Regulations

All Hands On Deck! Transition successfully to the new EU IVD Regulations
Tuesday, May 19 | 11-11:30 a.m. EDT (US) 4-4:30 p.m. (London)

The new EU IVD Regulations (EU 2017/746) bring a significant impact on all IVD manufacturers with a new risk-based classification and a greater emphasis on patient safety.

About 80% of all devices will now require some form of conformity assessment by a Notified Body, impacting every part of your organization and all its economic operators.

Join our experts for a webinar to discuss how early planning and a holistic organizational approach to implementing the changes will help you be ready in time, as well as

This is an opportunity to also hear from you and share your experiences.

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