Slides and replay immediately available!

By now you probably know that Class II device labelers have to comply with the FDA’s Unique Device Identification (UDI) mandate by September 24 of this year. If you didn’t know that and your organization labels Class II devices, you have some catching up to do! Lucky for you, my friends at Reed Tech will help companies who are behind schedule or have encountered problems as they try to meet the FDA’s UDI deadline.

Reed Tech UDI expert Gary Saner will help you understand where you should be in the UDI process and what you can do to get back on track. All is not lost, but I highly suggest attending this webinar for help getting started, restarting a stalled UDI compliance program, or if you’re finding you just need a little extra support along the way.

Register now to learn:
• Steps to comply
• UDI News
• Best Practices
• Project Timelines
• Submission Option Pros and Cons

Who should attend?
• UDI Team Leaders/Members
• Regulatory Leaders/Teams
• Manufacturing, Operations and Supply Chain Logistics
• UDI IT Support
• Distributors with UDI Submission Responsibilities

If you have Class I devices and you’re a real go-getter, you may want to start your planning by attending as well.

BONUS! When you register below, you’ll get immediate access to seven very popular UDI presentations Reed Tech made for the Medical Devices Group.

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