Healthcare IT News October 21, 2024
Jessica Hagen

The Agency says AI can transform multiple aspects of healthcare, but it is difficult to fully oversee and regulate the technology without the assistance of all sectors involved.

The Food and Drug Administration (FDA) has released its perspective on regulating AI in healthcare and biomedicine, stating that oversight needs to be coordinated across all regulated industries, international organizations and the U.S. government.

The Agency says it regulates industries that distribute their products to the global market, and therefore U.S. regulatory standards must be compatible with international standards.

It highlighted that it is working to accomplish this by coleading an AI working group of the International Medical Device Regulators Forum that both promotes AI best practices globally and leads...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: AI (Artificial Intelligence), FDA, Govt Agencies, Regulations, Technology
Device industry scrambles as FDA job cuts cause delays
FDA approves first rapid-acting insulin biosimilar for diabetes
Device industry scrambles amid concern FDA layoffs will cause delays
First Insulin Aspart Biosimilar Receives FDA Approval
In FDA job cuts, experts see threat of far-reaching impact

Share This Article