The bill prohibited the FDA from enforcing regulations aimed at increasing traceability of the supply chain, among other ...

The FDA plans to eliminate comparative clinical study requirements that currently add $24 million and up to eight years to ...

FDA Section 524B transformed medical device cybersecurity from guidance to law, challenging small medtech firms with ...

In June 2025, the US Food and Drug Administration (FDA) issued a final guidance titled Cybersecurity in Medical Devices: Quality System ...

Drug & Device Team provides recommendations based on Food & Drug Administration (FDA) draft guidance on Quality Management System ...

SNAP food benefits are flowing again after a pause during the federal government shutdown. But the clock is about to start on ...

The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries.

Through substantial leadership turnover and workforce cuts, the FDA has continued to support the advanced therapy sector, ...

In an interview with Targeted Oncology, Frederick L. Locke, MD, discussed how the elimination of the REMS program for CAR T-cell therapy came about and what effects he hopes this will have on patient ...

The Democrats weakened the borders, allowing Mexican drug cartels to smuggle fentanyl into the United States, where it ...

The U.S. Food and Drug Administration can approve new personalized treatments for rare and deadly genetic diseases based on ...

Earlier this fall, the FDA issued a reminder to pet food manufacturers to consider the highly pathogenic avian influenza H5N1 in their food safety plans as H5N1 cases tend to increase during the fall ...