EU MDR Webinar Featuring USDM's Jay Crowley

by Dalton Litzelman, on October 17, 2019

In the health care sector, medical device labeling is one of the most essential processes in production. Any slight error in your labeling could pose risk towards your patients, and, if you are not compliant with regulations, you could have painful recalls and fines. Because labeling requirements are hard to keep up with due to their fast-changing nature, you may be wondering if you are compliant with the information on your medical device label.

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) to comply with the European Union Medical Device Regulation (EU MDR). Also, with a new installment of label requirements it’s more than likely that you will need to make changes to the content on your device labels. When is the last time you investigated your labeling process to ensure compliance with EU MDR?

Fortunately, it is not too late to enhance your labeling practices and achieve EU MDR compliance. Loftware will be hosting a live webinar taking place on Thursday, October 24th, 2019 from 2 PM ET – 3 PM ET. If you want more information about EUDAMED and Labeling Requirements for EU MDR, you won’t want to miss this webinar. Topics of discussion include:

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

In this webinar you will hear directly from Jay Crowley, the Vice President of Unique Device Identification at USDM. Prior to joining USDM Jay was a 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. Representing Loftware in the webinar will be Joe Farrell. Joe has spent a bulk of his career selling automated supply chain solutions to the Life Sciences industries.

Attend this special webinar and discover everything your need to know about EU MDR and how you can stay complaint. Register for the webinar “EUDAMED and Labeling Requirements for EU MDR Compliance” today. Also, visit this blog post 5 Questions Answered About the New EU MDR.

Download EU MDR Report

Topics:Medical Devices