Exporting to Europe: Updates on the EU’s Medical Device Regulation

10:00 – 11:00AM EDT

Attention Georgia MedTech Companies!
A Second Chance to Tackle & Learn More About the European Union’s Medical Device Regulation (MDR) EU MDR Delayed by 1 Year

What does this delay mean for your sales in Europe and can it impact market entry and compliance?

Register: Click Here
GDEcD’s International Trade Division is offering a complimentary webinar to help Georgia medical device companies better understand the European Union’s new Medical Device Regulation (MDR).

The EU MDR is the largest overhaul to the regulatory framework governing medical devices in 30 years. The Medical Device Regulation will replace the Medical Devices Directive, which was originally slated to go into effect on May 26, 2020. Due to the COVID-19 pandemic, calls from industry were answered to delay its implementation.

The new MDR rulebook is comprised of 174 pages and will change the regulatory landscape in Europe; it will address technological advancements and focus on a life-cycle approach to medical device regulation and compliance.

Did you know: According to the US Commercial Service, more than $20 billion in medical devices were exported from the US to the EU in 2018, which corresponds to 38% of the total export market.

Join us, as we bring together a group of experts who will discuss the intricacies of these regulations and impart their insight on how your products can be marketed, distributed and sold in Europe.

For more information, contact Maxine Bier ([email protected]).

Learn more about Georgia’s International Trade Division at Georgia.org/Trade.