This free, one hour webinar hosted by Reed Technology will provide attendees updated information regarding the FDA’s Unique Device Identifier (UDI) and discuss strategies to implement your UDI submissions solution. Time is allotted for Q&A.

TOPICS FOR DISCUSSION:
• 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