EUDAMED and Labeling Requirements for MDR

For many medical device manufacturers, there is still some uncertainty about what data needs to be submitted to the European Database on Medical Devices (EUDAMED) in order to comply with the European Union's Medical Device Regulation (MDR). There are also new label requirements, which means most manufacturers will need to make changes to account for additional label elements.

Watch the following webinar to get a better understanding of what you need to do prior to May 26, 2020 and how an Enterprise Labeling Solution can help.

This webinar features topics such as:

Devices impacted by MDR
Types of data that must be submitted to the EUDAMED
Label implications and requirements
Connecting MDR data to your labels across your Enterprise and Supply Chain
Enterprise Labeling Solutions overview
Timelines and strategies

Presenters:

Jay Crowley, Vice President of Unique Device Identification for USDM. Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.

Joe Farrell, Labeling Specialist at Loftware. Joe has spent the bulk of his career selling automated supply chain solutions to the Life Sciences industries.

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