Dr. Fatima Sanfourche

Senior Manager RA/QA Compliance for Medical Devices and eHealth Bayer

Conference Day 2

Explore major changes of vigilance systems due to the MDR requirements
Discuss how these regulations introduce an EU identification system for medical devices based on a Unique Device Identifier
Consider the role of UDI in the traceability of the device during the vigilance reporting process
Analyse the challenges of the implementation of the new electronic reporting process
Deep dive into how UDI will enhance the effectiveness of post-market safety-related activities for devices

Check out the incredible speaker line-up to see who will be joining Fatima.

Address: IQPC Ltd, 129 Wilton Road,
London SW1V 1JZ
Telephone: 44 (0) 207 368 9300
Fax: 44 (0) 207 368 9301
Email: enquire@iqpc.co.uk