Demystifying IEC 81001-5-1 and Cybersecurity Testing for Medical Devices
Access our expert webinars that could transform your Go-to-Market strategy!
The medical device industry is evolving fast, and staying compliant is more than a checkbox. It’s a competitive advantage.
TÜV Rheinland brings you two exclusive, expert-led webinars that dive deep into the critical standards and cybersecurity requirements shaping today’s regulatory landscape in the USA and European Union.
Whether you’re launching a new product or improving an existing one, these sessions are packed with must-know insights to keep you one step ahead.
This webinar series covers key topics, including:
Cybersecurity Testing for Medical Devices
Discover how to design and test medical devices with cybersecurity built in. From understanding regulatory expectations (FDA, MDR) to implementing robust security measures, this session covers the essentials for delivering secure, compliant technologies in a connected world.
IEC 81001-5-1 & Global Compliance
Learn how to navigate IEC 81001-5-1 and related standards like IEC 60601, EMC IEC CB reports, REACH, and RoHS. Designed for devices sold in the US and EU, this webinar provides clear guidance on ensuring safety, interoperability, and legal compliance.
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