PranaX Corporation ( an emerging regenerative medicine biotechnology company, today announced that it has licensed exosome technology from The University of Texas MD Anderson Cancer Center to develop ...

I was not aware of it, and I should have been.”After a rise in complaints, in 2020 the FDA required drug manufacturers to add ...

ILUVIEN now approved for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye (NIU-PS) in addition to ...

The FDA approved a prefilled syringe format for Ani's purified Cortrophin Gel that should ease administration for MS patients ...

The US Food and Drug Administration on Thursday issued recommendations for the composition of influenza shots for the ...

Eton Pharmaceuticals (ETON) announced positive results from its bioequivalence study of ET-600, a proprietary, patented oral solution of ...

Joseph Borzelleca published a study on food coloring Red No. 3. The FDA cited his work when banning the additive in January.

The combination drug could help around 1,000 women every year in England who suffer from the debilitating condition. | ITV National News ...

The drug, also called Relugolix, blocks signals from the brain that tell the ovaries to make oestrogen, a hormone that fuels ...

Some major decisions on the future of reproductive rights and access to abortion are active in our courts right now. Some of ...

Spineart and eCential Robotics today announced the receipt of FDA 510(k) clearance for the use of an application for robotic ...

The Senate Committee on Health, Labor and Pensions voted Thursday to approve Marty Makary as commissioner of the Food and Drug Administration. He will likely be confirmed in the full Senate.