UDI Conference 2014
October 28-29, 2014
Hilton Baltimore - Baltimore, Maryland
The annual UDI Conference is the ONLY event dedicated to guidance and training for those impacted by the new UDI Regulation:
- Medical device manufacturers
- Health care distributors
- Group purchasing organizations
- Hospitals and health care providers
- Health care industry professionals
The FDA UDI Regulation establishes a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required to comply with the new UDI methodology.
Learn how device manufacturers, distributors, and hospitalswill be able to facilitate the following with a UDI system:
- Reduction of Medical Errors
- Supply Chain management
- Utilization of UPN and PDU data
- Recall of Medical Devices
- Improved Medical Device Reports (MDRs)
- Preventing Allergic Reactions to Devices
- Identification/Reduction of Product Counterfeiting
- More Efficient Purchasing
- Improved Inventory Control
- Enhanced Medical Device Asset Utilization
- Efficient Reimbursement
- Identification of Compatibility Issues
- Enhancements in Post-Market Surveillance
You can also explore the technology behind UDI in the exhibits area where you can learn about the solutions for your UDI implementation.
Join us at Booth 15, and see how our solutions can work for you.
For more information about this event on the UDI Conference website.
