The Post Market Surveillance: Regulatory requirements & practical implications

Upon the entry into force of the European Medical Device Regulation (MDR), the implementation of an effective Post-market surveillance system, proportionate to the risk class and appropriate for the type of device, has become a pivotal requirement for manufacturers.

This webinar will provide an in-depth understanding of the key requirements, concepts, and the overall process for post-market surveillance under the MDR.

The session will explore the implications of applicable MDCGs, offering valuable insights and practical guidance for adapting your internal procedures and ensuring medical device compliance with MDR requirements.

Registration is only granted to medical device company manufacturers and partners.