Back by popular demand!
The first installation of this excellent webinar had so many questions that we went 30 minutes longer than planned. This second one-hour webinar hosted by Reed Technology will provide you with more in-depth information regarding the FDA’s Unique Device Identifier (UDI) and discuss strategies to implement your GUDID submissions solution.

TOPICS DISCUSSED:
• An update on the FDA UDI requirements for Medical Device Manufacturers (Labelers) based on the FDA’s Final Rule and Guidance for Industry
• UDI basics to guide your organization in meeting the UDI Regulation
• Timelines of upcoming FDA Guidance and Device Compliance Dates
• Critical updates you need to know pertaining to the UDI ruling

WHO SHOULD ATTEND:
• UDI Team Leaders/Members
• Regulatory Directors/Managers/Staff
• Manufacturing, Operations, and Supply Chain Logistics Personnel
• UDI IT Support Personnel
• Compliance Officers
• Distributors with UDI Submission Responsibilities