The US FDA has warned Sanofi about significant deviations from Current Good Manufacturing Practice for active pharmaceutical ingredients.

Good morning! Here are the five things you need to know in local business news to start your busy — and still very cold — ...

The FDA has warned Sanofi about a series of “significant” manufacturing problems, including contamination, at a key facility ...

Despite receiving a prior wrist slap from the FDA in the shape of a Form 483, Sanofi is still working to right the ship at a ...

Officials cited a statute known as the Delaney Clause, which requires FDA to ban any additive found to cause cancer in people or animals. The dye is known as erythrosine, FD&C Red No. 3 or Red 3.

An FDA proposal Wednesday calls for drastically ... but a snowmobile group in Massachusetts is looking to bring supplies to communities in need. Dress for Success Western Massachusetts is ...

Jan. 14 (UPI) --The U.S. Food and Drug Administration hopes "front-of-package" labeling will better improve the American population's health, the FDA announced. "Food should be a vehicle for ...

Fox News correspondent Molly Line joins 'America's Newsroom' to discuss federal immigration shelter inspections taking place in Massachusetts following a major drug and weapon bust. Trump takes ...

There have been no reported illnesses linked to the cheeses. The FDA said the products were sold at stores in Colorado, Massachusetts, Maine, New Hampshire, and Ohio. The retailers and distributors ...

There have been no reported illnesses linked to the cheeses. The FDA said the products were sold at stores in Colorado, Massachusetts, Maine, New Hampshire, and Ohio. The retailers and distributors ...

WALTHAM, Mass.--(BUSINESS WIRE)--Revvity, Inc. (NYSE: RVTY), today announced that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for EUROIMMUN’s automated ...