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.

Join us for a comprehensive webinar 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 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

We look forward to seeing you there!