Henry Schein: UDI Data Submission Case Study


UDI Data Submission

Jeff Peacock, VP of Global Quality Assurance and Regulatory Affairs at Henry Schein, gives industry members an overview of how his organization approached the challenge of UDI data submission to FDA.

Download the guide to learn about:

  • The challenges presented by the UDI data submission mandate
  • How Henry Schein approached the problem of data collection and standardization
  • Why Henry Schein chose the Reed Tech UDI system (SingleSource(TM) for Medical Devices) as their solution

“When considering the value of the Reed Tech system, I think the price is well worth the cost.” -Jeff Peacock, VP of  Global Quality Assurance and Regulatory Affairs, Henry Schein, Inc. 

Questions? We are here to help. Visit our Knowledge Center or Contact Us.