Decoding regulatory realities for innovations in medical devices

July 02, 4:00pm CET
Online

Compliance Standard Regulation Image Medical Device Regulation

How do you turn EU regulations into daily practice?

EU substance regulations are evolving with direct impact on medical device compliance. This 90-minute webinar unpacks how classification under REACH connects to EU MDR requirements and what it means in practice. Learn to navigate key concepts towards MDR-compliance, explore testing approaches, and see how regulatory insight can drive smarter material and innovation decisions.

Key insights

The regulatory path of substances in EU
Beyond compliance: from reactive response to proactive responsible chemistry
MDR-compliance of reactive materials in practice
Regulation-innovation cycle

Featured speakers

Claudia Hoelscher
Head of Product Safety & Regulatory Affairs
LinkedIn

Hermann Handwerker
Senior Principal Application Engineer

Kanako Nishino
Biological and Clinical Evaluation Expert, Pro-Liance
LinkedIn

Thomas Brzoska
Managing Director, Pro-Liance
LinkedIn

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Decoding regulatory realities for innovations in medical devices

How do you turn EU regulations into daily practice?

Key insights

Featured speakers

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Personal details

Mobile verification

Company details

Looking for solutions? We can help

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