With less than three months until the September 24 deadline for Class III UDI / GUDID Submissions, Class III device manufacturers in the early stages of GUDID compliance activities must move forward quickly. Additionally, many Class II and implantables manufacturers must soon begin to implement UDI compliance to meet original equipment manufacturer (OEM) and customer demands.

The UDI / GUDID Compliance Webinar will focus on the necessary steps for submission to the GUDID. Reed Tech subject matter expert Gary Saner will cover the following topics in detail:

• UDI Compliance Deadlines
• GUDID Submission Methods and Approaches
• GUDID Account Set Up Process
• DUNS numbers
• GUDID Data Attributes
• Approved Issuing Agencies

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