MEET GLOBAL INDUSTRY REQUIREMENTS WITH 1WORLDSYNC PRODUCT CONTENT SOLUTION
At 1WorldSync, we enable healthcare organizations to simplify and manage the process of exchanging global commercial regulatory information.
We help you to meet industry requirements and regulatory demands and turn them into a competitive advantage:
- Close collaboration with organizations like the European Commission, NHS and MedTech Europe (European Association of Medical Device Manufacturers)
- Many years of experience with the FDA GUDID connection
- Operating the NHS data pool
- Global visibility on product content exchange projects e.g. AGKAMED (Germany), RESAH and GAM (France), Dutch Implant Registry, Spanish hospitals
Upcoming industry compliance deadlines:
Why is MDR important to you?
In April 2017 the European Parliament approved the MDR regulation mandating UDI registration in Europe. More information.
Have you selected your GDSN data pool yet?
In January 2017 NHS confirmed to continue with GDSN implementation plans. All NHS suppliers have to select a GDSN data pool in order to deliver product content to NHS. More Information.
Are you prepared for upcoming UDI regulations?
In order to comply with US FDA UDI regulation, your product data must be stored in the GUDID. More Information.
We are global. Helping more than 25.000 global brands in more than 60 countries, our Healthcare Experts understand that no matter where you conduct business, trusted content matters.
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.
- Holger Clobes, B. Braun