Henry Schein: UDI Data Submission Case Study
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.
The opinions expressed within this case study represent customer opinions. Reed Tech believes this case study experience generally represents the experience found with other similar customer situations. However, each customer will have its own subjective goals and requirements and will subscribe to different combinations of Reed Tech services to suit those specific goals and requirements. This document is for educational purposes only and does not guarantee the functionality or features of LexisNexis Reed Tech products identified. LexisNexis does not warrant this document is complete or error-free. This case study may not be deemed to create any warranty or representation that other customer’s experience will be the same as identified herein.
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