How to Prepare for EU MDR 2020

Join us for a 60-minute webinar, “Insight from Experts and Medical Device Manufacturers,” with live Q&A on Wednesd

Register at tiny.cc/vkc46y

Wednesday, May 29, 2019 at 11:00 AM PT / 2:00 PM EDT

In less than one year, the Medical Devices Regulation (MDR) will be fully implemented. As of May 2020, medical device manufacturers that wish to distribute products in the European Union will be required to comply with these new rules. For these organizations, there is a lot to do to prepare in a relatively short time. In this webinar, you’ll learn valuable insight from industry experts and medical device manufacturers on how to be fully prepared for this important regulatory change.

Join Michael Drues, recognized Life Sciences expert; Maite Llacer, Director, EU Vigilance at Edwards Life Sciences; Angeles Sanfrancisco, Manager, EU Vigilance at Edwards Life Sciences, and Kim Wakeman, Life Science Solution Expert ETQ to learn:

Overview of EU MDR regulations timeline and scope Where most organizations stand with their compliance journey today Major areas of the Regulations Annexes EU MDR Product Vigilance Lessons learned and best practices How organizations can determine their readiness