food and drug administration

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Kraft Heinz Is Removing All Artificial Food Dyes

One of the world’s largest food companies pulls certain artificial dyes from US products

Health advocates have long called for the removal of artificial dyes from foods, citing mixed studies indicating they can cause neurobehavioral problems, including hyperactivity and attention issues,...

· 3h · on MSN

Food giant Kraft Heinz vows to stop using artificial dyes

· 1h

Kraft Heinz to remove all artificial dyes by end of 2027

· 1h

Heinz rolls out plan to halt use of food dyes in two years

The Food and Drug Administration already banned Red Dye No. 3, which will take effect in 2027.

abc7NY · 4h

Kraft Heinz will remove all artificial dyes from its foods, complying with RFK Jr.'s demands

· 5h

Kraft Heinz to remove artificial dyes from U.S. products by end of 2027

42mon MSN

US FDA to shorten review time for drug developers under new voucher program

The U.S. Food and Drug Administration said on Tuesday it is launching a program under which its commissioner can issue vouchers to companies to shorten their review time for a drug application to 1-2 months from the typical timeline of about 10-12 months.

1hon MSN

New FDA Chief Wants to Fast-Track Some Drugs, Use More AI

And offering a fast-track to approve drugs the Trump administration views as a priority. Welcome to the new Food and Drug Administration as envisioned by Dr. Marty Makary, who is leading the agency under Health Secretary Robert F.

55m

US FDA to Issue New Vouchers to Drug Developers to Shorten Review Time

(Reuters) -The U.S. Food and Drug Administration on Tuesday announced that it will issue a new priority review voucher to drug developers to shorten review time from about 10-12 months to one-two months.

7hon MSN

We Spent a Year Investigating How the FDA Let Risky Drugs Into the U.S. Market

Our investigation exposed a little-known practice inside the FDA that allowed more than 150 drugs or their ingredients into the U.S. over the past dozen years even though they were made at factories banned from shipping their products here.

A new chapter for online sales of obesity drug alternatives tests legal limits

While some compounding pharmacies have stopped making alternatives to Wegovy and Zepbound since shortages were declared over, others are continuing and pushing regulatory boundaries.

FDA Plans to Use AI to Speed Up Drug and Food Safety Reviews

WEDNESDAY, June 11, 2025 (HealthDay News) — The U.S. Food and Drug Administration (FDA) says it plans to use artificial intelligence (AI) to help speed the approval of new drugs and medical devices. That's one of several priorities federal officials detailed June 10 in JAMA.

MIT Technology Review4d

Here’s what food and drug regulation might look like under the Trump administration

Leaders of the FDA have published a list of new priorities for the agency. They want to deliver rapidly-approved cures and "unleash AI."

Capricor Therapeutics' Becker Muscular Dystrophy Drug Gets Orphan Drug Designation in U.S.

Capricor Therapeutics has received an orphan drug designation for its drug aimed at potentially treating Becker Muscular Dystrophy. The biotechnology company said Tuesday that the Food and Drug Administration granted the special status to Deramiocel, the company's lead cell therapy candidate.

What Makes a Food Ultraprocessed? The FDA Is About to Weigh In.

That description could then be used to shape school lunch policy, regulate the foods available through federal services like the Supplemental Nutrition Assistance Program or make recommendations about limiting ultraprocessed food consumption in the U.