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.
-
-
-
-
Every question, request, and challenge is an opportunity for us to help your business perform. And we have all the right people ready to make it happen.
Check our FAQ for quick answers or reach out via phone to our support center. Here, we also offer additional inquiry forms to help you connect with the appropriate Henkel expert.