Are you ready for Unique Device Identification (UDI) compliance?
UDI Educational Assets and Events
|UDI for 2018: Why You Should Start Now!||Read Now|
|UDI: Generating Value Beyond Compliance||Read Now|
|UDI: One Cost for Compliance. Advanced Readiness||Read Now|
|Will You Meet the Compliance Deadline?||Read Now|
|Case Study: Teleflex||Read Now|
|Webinar- GDSN for UK NHS eProcurement & Buyer Data Requests||Recording
|Webinar- June 15, 2017 11:00am EDT
UDI: Why You Should Start Now!
|Recording: UDI Compliance and What You Need to Know||Watch Now|
|Webinar- June 14, 2017 12:00pm EDT
Why Your Data Needs to be in the GDSN
A Seamless and Proven Process
We understand that the product information you're sharing resides in multiple places, formats and systems, and is even controlled by different functions. That's why we provide a seamless and proven process to collect, store, manage, and distribute product information, whether it's for your customers, trading partners or for compliance with the UDI regulation. Our experts will help identify and create a sustainable process to successfully publish UDI compliant product information to the Global Unique Device Identification Database (GUDID). Best of all, our direct integration with the GUDID eliminates the need for your business to build a dedicated pipe.
1WorldSync is the industry leader in global transparency and compliance solutions. Global regulations, similar to UDI, are currently in development in Europe and Asia that could impact your business. 1WorldSync is poised to support your business for global compliance to current and future healthcare supply chain regulations.
"1WorldSync helped streamline our internal processes and create a single source of truth, ensuring we had the accurate and complete product information in time for the Class III UDI compliance deadline. This scalable model is currently working to prepare 8,000 products for Class II and over 10,000 products for Class I."
If you're like us, you like to be ahead of the game. With the 1WorldSync UDI Solution your business can prepare and validate medical device product information before the compliance deadline, giving you more time to focus on producing the quality products your customers and patients love.