Does your company manufacture or market medical devices in the European Union? Then you’re probably aware of the upcoming implementation of the EU Medical Device Regulations in May of 2020. And for IVD manufacturers, the new In Vitro Diagnostics Regulation goes into effect May of 2022. But whether you have four months or two years to prepare, you must be educated on the new regulations, which will modernize the processes by which medical devices and IVDs come to market.
Luckily, anyone struggling to prepare for these changes can attend the upcoming Medical Design & Manufacturing West 2020 Conference on February 11, which will hold sessions aimed at preparing manufacturers and marketers for the EU MDR and IVD. Speaking at the conference will be regulatory affairs specialists from the following companies:
Edwards Lifesciences
Zap Surgical
Abbott
Agendia
BSI Medical Devices
NSF International
Kim Walker Consulting
The following paid conference sessions will be held in Room 210D:
10:45 – 11:45: Panel Session: Strategies for Implementing the New EU MDR Requirements
1:15 – 2:00: EU MDR & IVD Compliance: Tales from the Trenches
2:05 – 3:00: How to Design an Easy to Maintain Risk Management System
3:15 – 4:00:The Impact of IVDR Requirements on Manufacturers and Strategies
Presented by Corey Cashmere, a free conference session on EUDAMED will be held at Tech Theater, Booth 637 on Thursday at 1:30 pm.
The conference will be held from February 11-13, 2020 at Anaheim Convention Center in Anaheim, California.
For medical device compliance testing, contact us for a quote. Rhein Tech is a conveniently located EMC testing lab in Herndon, Virginia, offering competitive prices, quick testing, and individualized services.