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 ...

On June 2, 2017, the US Food and Drug Administration (FDA) announced that it plans to delay the dates by which certain Class I devices and unclassified devices must comply with the agency’s 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.

FDA has announced it has proposed that most medical devices distributed in the United States carry a unique device identifier, according to a news release. The announcement comes in response to ...

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 ...

A week after federal legislators and hospitals pressed the Office of Management and Budget about the release of a final unique device identification rule, the U.S. Food and Drug Administration ...

QAD ERP Makes it Simpler to Achieve UDI Regulatory Compliance and Ensure Product Integrity from Component to Patient with Backward and Forward Traceability <0> QAD Inc.Ashley DeVan, +1-805-566-6126Sr.