MakroCare is organizing the webinar on Medical Device PMS & PMCF: Challenges & Opportunities. This webinar will focus on pitfalls and challenges in planning, conducting, and managing PMCF studies.

The new 2017/745/EU Medical Device Regulations (MDR-2020) require increased emphasis on Post- Market Clinical Follow-Up (PMCF) as a part of clinical evaluation to demonstrate conformity to safety and performance of devices.

Speaker:
Mary Majer
Clinical Subject Matter Expert, Medical Devices

Date & Time: Thursday, July 12, 2018 | 11am US EST / 4pm EU CET

Click here to register : https://www.makrocare.com/webinar-registration-for-medical-device-pms-pmcf-challenges-opportunities