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FDA PUBLISHES UDI PROPOSAL
The U.S. Food and Drug Administration (FDA) recently announced that it is amending the implementation timeline associated with its previously proposed unique device identification (UDI) rule.
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Michael Ward, Loftware's Vice President of Technical Services, explains how customers are leveraging the Universal Connector's powerful, configurable business logic to boost supply chain efficiency and reduce costs.
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Fill out the form below to view the webcast recording.
View the Webcast Recording:
UDI Requirements & the FDA — Now is the Time to Act!
Featuring: Jay Crowley, FDA Senior Advisor for Patient SafetyLoftware and Jay Crowley, FDA Senior Advisor for Patient Safety, joined forces to discuss the upcoming FDA and Unique Device Identification (UDI) requirements and their overall impact on the medical device industry.
In this webcast, Jay Crowley went over new updates from the FDA regarding UDI requirements and how these changes will:
- Increase patient safety
- Impose more effective recalls
- Enhance post market surveillance
- Improve clinical operations
- Elevate supply chain efficiency
Fill out the form to the left to download the recording and learn how this proposed regulation not only affects your business, but how most medical device manufacturers have invested heavily to streamline their operations to compete globally and meet the future FDA requirements.
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