FDA's Diamantas: Defining ultra-processed foods is ‘really hard’

Food and Drug Administration Deputy Commissioner for Food Kyle Diamantas said his agency's agenda has support "from the very ...

US FDA approves Merck's pill combo to treat HIV infection

By Christy Santhosh and Sriparna Roy April 21 (Reuters) - The U.S. Food and Drug Administration has approved Merck's ...
Axios on MSN

Drug ads face new scrutiny at FDA and on Hill

Prescription drug commercials are facing renewed scrutiny as the Trump administration and lawmakers from both parties seek ...

Oncologists vs. the FDA and RFK Jr.

Doctors who treat melanoma are shocked by a drug’s rejection.

Pfizer and Astellas secure FDA priority review for Padcev MIBC combo therapy

Pfizer and Astellas have received the US Food and Drug Administration (FDA) acceptance for priority review of their ...
Regulatory Affairs Professionals Society

FDA warns firm for inappropriate use of AI in drug manufacturing

The US Food and Drug Administration (FDA) has issued a warning letter to Purolea Cosmetics Lab for several violations of Good ...

Belite Bio Initiates Rolling Submission of New Drug Application to the U.S. Food and Drug Administration for Tinlarebant for the Treatment of Stargardt Disease

Belite expects to complete the new drug application submission in the second quarter of 2026Rolling submission initiated ...

Norovirus fears prompt FDA warning to restaurants and retailers: Stop selling this recalled shellfish

A safety alert came on Friday after health officials in Washington State reported illnesses associated with the consumption ...
Regulatory Affairs Professionals Society

FDA draft guidance sets impurity controls for most antibiotics

The US Food and Drug Administration (FDA) has released a draft guidance document aimed at setting impurity limits for ...
Rheumatology Advisor

FDA Expands Caldolor Use to Include Postoperative Pain Management

FDA expands Caldolor (ibuprofen) injection indication to include postoperative pain in adults and pediatric patients (3 months+).
IndiaWest

FDA Flags Indian Drug Maker Lupin’s NJ Plant

SOMERSET, NJ -Major drug maker Lupin said on April 18 that the US Food and Drug Administration (USFDA) has issued a ‘Form 483 ...

One Year Later: Are Synthetic Dyes Still in Our Food?

The federal government made a big announcement about phasing out artificial food dyes. Here’s what has happened since.