Watch Now

On-Demand Webinar

The evolving global UDI regulations, coupled with commercial device identification and information requirements such as the UK NHS requirements, are prompting companies to re-assess their Master Data Management (MDM) strategies.  In this webinar, we will explore these new requirements, discuss how they affect your current and planned UDI and MDM programs, and highlight ways to address these challenging requirements.  

The discussion will include:
  • Highlights of key requirements: Global UDI, UK NHS, key commercial requirements
  • Impacts on existing UDI and MDM programs
  • How to address these requirements
  • Live Q & A session
About the Presenters:
Jay Crowley
Jay Crowley

Vice President of Medical Device Solutions and Services 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.

Grant Hodgkins
Grant Hodgkins

Vice President of the ERP, PLM and Track & Trace Services and Solutions at USDM Life Sciences With over 30 years of experiences in the Life Sciences, Grant assists USDM Life Sciences clients with Pharmaceutical Track and Trace, Enterprise Resource Planning (ERP), Product Information Management (PIM), Product Lifecycle Management (PLM), Manufacturing Execution Systems (MES) and other commercial enterprise solutions.

Want our experts to work on your project?

Take the first step towards creating more value with USDM today.

Connect Now

We use cookies to understand how you use our site and improve your experience. This includes personalizing content and advertising. Learn more.