On-Demand Webinar:
What You Need to Know About Establishing a UDI System
Is this webinar right for you?
This webinar is perfect for you if you're a medical device manufacturer or health care distributor.
The FDA's new Unique Device Identification (UDI) regulation says that if you manufacture medical devices, you're required to comply on or before September 24th, 2020.
But are you ready to embrace a UDI system?
Watch our on-demand webinar and learn how to develop a UDI roadmap and implementation strategy.
You'll also learn how:
- Comply with the new regulations
- Reduce medical errors
- Manage your supply chain
- Recall medical devices
- Improve Medical Device Reports (MDRs)
- Identify and reduction product counterfeiting
- Improve inventory control
- Enhance post-market surveillance
Ready to Watch?
To receive access to this on-demand webinar, please fill out the form on this page and we'll deliver it straight to your inbox.
