Today, the U.S. Food and Drug Administration (FDA), in partnership with the National Institutes of Health National Library of Medicine (NLM), is making data on devices with unique device identifiers ...

The FDA is in the process of implementing the Unique Device Identification (UDI) System in a series of phases. Currently, all Class III and implantable, life-supporting and life-sustaining medical ...

In case you didn’t think number crunchers are taking over the world in the age of Big Data, artificial intelligence and “deep learning,” the feds just handed them another victory, this time in the ...

Please provide your email address to receive an email when new articles are posted on . The FDA is granting an extension for soft contact lens labelers to comply with the requirements of the Unique ...

A recent blog post in the reSOURCEs section of the HealthTrust public website discusses how the new UDI system will affect healthcare operations. In 2013, the U.S. Food and Drug Administration (FDA) ...

The healthcare supply chain has seen its share of ups and downs this year. In the early months of the COVID-19 pandemic crisis, product shortages were exacerbated by a lack of supply-chain visibility.

The Healthcare Supply Chain Association has announced it submitted its final comments to FDA regarding the proposed rule to establish a Unique Device Identification System for medical devices, ...

The Food and Drug Administration last week released an amendment to its proposed rule for a unique device identification system released in July. The amendment shortens the originally proposed ...

The Obama Administration’s Office of Management and Budget has approved and released a long-awaited proposed rule on a unique device identification system for medical devices. The document was ...