The Food and Drug Administration sends warning letters to entities under its jurisdiction as part of its enforcement ...

The U.S. Federal Trade Commission (FTC) announced last week that it is, for the second time, disputing hundreds of “junk” ...

An investigation published by The BMJ today raises concerns about financial entanglements between US Food and Drug ...

The H5N1 bird flu has been common across wild bird populations for the last few years leading to the culling of millions of ...

Prescription Drug User Fee Act (PDUFA) goal date extended by three months for further review of submission to August 14, 2024COPENHAGEN, ...

Cue Health Inc. (Nasdaq: HLTH), a healthcare technology company (the "Company"), has received a warning letter from the FDA about its Emergency Use Authorized (EUA) COVID-19 test. The Company is ...

Food and Drug Administration (FDA) Commissioner Dr. Robert Califf testified on oversight matters before the House Oversight and Accountabili… read more Food and Drug Administration (FDA ...

I write about healthcare policy, with an emphasis on Rx drugs. Two weeks ago, the Food and Drug Administration approved Xolair (omalizumab) for immunoglobulin E-mediated food allergy in certain ...

On December 26, 2023, the Food and Drug Administration (FDA) issued a Small Entity Compliance Guide Final Guidance Document: Direct-to-Consumer Prescription Drug Advertisements: Presentation of the ...

Navigating the complex landscape of drug approval presents significant regulatory challenges, requiring a delicate balance between fostering pharmaceutical innovation and ensuring patient safety. The ...

Marijuana legalization, or at least decriminalization, is picking up steam. Further moves could reshape the future of drug ...