In a world of regulatory compliance, there has never been a more important time for the healthcare industry to address product information management.
Patient safety, medical device traceability and government regulations are having a profound effect on product information within the healthcare industry. The demands are growing and it is essential that healthcare companies find a comprehensive and cost-effective approach to manage, collect, validate and distribute information.
1WorldSync is the industry leader in global transparency and compliance solutions and a reliable source for authentic, enriched data to support regulatory compliance, improvements in patient safety and increased supply chain efficiency.
We help you to meet industry requirements and regulatory demands and turn them into a competitive advantage by leveraging:
1WorldSync supports your business’s global compliance with current and future healthcare supply chain regulations:
At 1WorldSync, we address patient safety and complex regulatory mandates through one synchronized platform. It’s no wonder why our healthcare community consists of the industry’s top brand owners, medical device manufacturers, distributors, GPO’s and providers.
The United States Food and Drug Administration (FDA) regulation mandates that UDI data for Class I medical devices to be submitted with an impending deadline of September 24, 2020. For organizations manufacturing medical devices, are you ready for these regulatory demands?
