Critics worry that the user fee program creates a conflict of interest between the FDA and pharmaceutical companies.

Generative Phosphoproteomics AP3 platform designed to enable streamlined, rational drug discovery, with proprietary, proteome-wide SAR delivering ...

Received Clearance from the U.S. Food and Drug Administration (FDA) for Clinical Trials of Budoprutug in Primary Membranous Nephropathy (pMN), ...

MELVILLE, N.Y., March 27, 2025 (GLOBE NEWSWIRE) -- BioRestorative Therapies, Inc. ("BioRestorative”, "BRTX” or the "Company”) ...

The HHS Secretary has issued a directive to stop a loophole that lets companies approve their own food additives. Here's what ...

Chairs were placed on the stage for U.S. Sens. Bernie Moreno and Jon Husted, both Republicans - they sat empty, and ...

Explore RFK Jr's push for GRAS reform and its impact on food safety. Experts David Acheson and Dr Darin Detwiler discuss ...

First approved therapy to address hyperphagia in individuals with Prader-Willi syndrome Management to host conference call and webcast today, March 26th, at 5:30pm ET REDWOOD CITY, Calif., March 26, ...

The headliners this week are the nominees to lead the National Institutes of Health and the Food and Drug Administration ... deliver,” Johnson said on the program “Sunday Night in America.” ...

AHRQ also works on a number of programs funded by Congress to address patient safety and health care mishaps, like a program aimed ... of workers at the Food and Drug Administration were told ...

Stakeholders have been asking for more time to comply with the rule, which creates a tracking system for food throughout the ...