The US UDI compliance deadline for class I devices is less than four months away. Will your company be ready to comply with the regulation? Join our webinar for some last-minute tips on how to ensure your devices are compliant. We’ll also discuss some common missteps device manufacturers made with class II and III devices and how to address them.
This presentation will include:
About the Presenters:
- Overview of UDI Final Rule for class I devices
- Class 1 compliance checklist
- Common UDI compliance missteps
- Tips to fix previous mistakes
- Live Q & A
Vice President of Unique Device Identification Solutions Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.