WARENSVILLE HEIGHTS, Ohio – The FDA has established a unique device identification system to adequately identify medical devices through their distribution and end use. When fully implemented, the label of most devices must include a unique device identifier in human- and machine-readable form. Device labelers must also submit certain information about each device to FDA’s Global Unique Device Identification Database.
While the UDI system will be phased in over several years, life sustaining, life supporting and implantable medical devices are required to be compliant by September 24. Learn the FDA’s expectation of labelers, dates that your devices must comply, and how to prepare the data required to be submitted to the FDA.
Speakers: JALEX Medical, Jennifer Palinchik, President
Melissa Spang, Quality and Regulatory Specialist
Location:
Corporate College East, 4400 Richmond Road, Warrensville Heights, OH 44128
Registration begins at 9 AM.
To register, click on Events
