CE Marking Essentials and Compliance for Medical Devices

Discover how to prepare your medical device for the EU market at our webinar, which covers CE Marking essentials and offers actionable compliance strategies.

THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

Watch now: CE Marking Essentials and Compliance for Medical Devices

Achieving CE Marking under the Medical Device Regulation (MDR) is a complex process. It requires a deep understanding of device classification, conformity assessment procedures, technical documentation, and increasingly, cybersecurity and wireless communication standards.

Webinar date: Nov. 25, 2025

Our comprehensive on-demand webinar is designed to help professionals in the medical device industry understand the journey of CE Marking. This session will provide an overarching view of the CE Marking process under the MDR, with a focus on both general and wireless-enabled devices.

Attendees of the on-demand webinar will learn about:

The general process and key steps of CE Marking for medical devices
The fundamental MDR requirements, such as device classification and technical file content
The process and key steps for wireless devices
Cybersecurity compliance

Moderator

Alex Martin Smith, Sales Manager, Consumer, Medical and Information Technologies, UL Solutions

Speakers

Maggie Chiu, Project Engineer, Consumer, Medical and Information Technologies, UL Solutions
Joaquin Gomez Serrano, EMC and Wireless Senior Product Specialist, Consumer, Medical and Information Technologies, UL Solutions
Aifa Taieb, Senior Project Engineer, Consumer, Medical and Information Technologies, UL Solutions
Fergus Wong, Cybersecurity Product Specialist, Consumer, Medical and Information Technologies, UL Solutions