FDA took issue with the promotional communication presented in an exhibit booth panel (“panel”) [2] for Hemady ®, a drug indicated in combination with other anti-myeloma products for the treatment of ...

USDA Secretary Rollins and HHS Secretary Kennedy announced that they are reviewing the current Dietary Guidelines for Americans report, which will be changed and released this year.

Specialty pharmaceutical company PharmaTher Holdings’ drug application for Ketamine has received a June 4 approval goal date, advancing approval of the drug in the U.S. PharmaTher said it is ...

Pharmaceutical consultants apply their comprehensive expertise in different areas to accelerate the drug development process.

Joseph Shea, who sells athletic wear in Myrtle Beach, South Carolina, wonders and worries about the food he eats.

Zepbound contains the same active ingredient, tirzepatide, as Mounjaro, which is also made by Lilly and is FDA-approved to treat Type 2 diabetes. Some doctors also prescribe Mounjaro "off-label" for ...

Leaders of USDA and the Department of Health and Human Services committed to releasing the final Dietary Guidelines for ...

Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...

Last month, a non-peer-reviewed study commissioned by Moms Across America alleged that Girl Scout Cookies had toxins in them.

Kratom is in a gray area of federal regulation, leaving it up to individual states to figure out how to control it.

The Health Secretary wants to eliminate a provision that allows companies to self-affirm that food ingredients are safe.

It’s time to revamp the FDA’s “generally recognized as safe,” or GRAS, program that allows companies to add untested ...