Achieving UDI Compliance – More Than Just a Label Change
In this 60 minute webinar Jay Crowley, Vice President of UDI Solutions and Services at USDM and Hal Plant from PRISYM ID present how you can best incorporate UDI into your overall quality, compliance and risk management strategy to not only drive UDI compliance but deliver significant productivity benefits.
Achieving FDA UDI compliance is not just about the label. This is just one element in the wider process of effectively managing data within the production process. With a high percentage of voluntary recalls of medical devices caused by labeling and packaging defects, it’s easy to see how the label becomes the focus. The implications of product recall are significant; efficiency, productivity, and ROI take a major hit, while the potential damage to brand reputation and patient safety are equally severe. However in striving to deliver safe, accurate and compliant product information, it’s not just about the label-it’s all about the data.
By taking a 360 view organizations can ensure that they capture, store, and disseminate data safely, quickly, and accurately. Centralized data creates a robust platform for a “single version of the truth” that can be used to support UDI compliance and provide an audit trail, ensuring the right information goes on the right product at the right time, every time.
Benefits of Viewing:
- Understand UDI requirements and your responsibilities
- Learn how to leverage UDI to reduce risk and drive new operational efficiencies
- Discover how to incorporate UDI into your overall quality, compliance and risk management strategy
- Achieve an insight into the impact of UDI on data management