The Delaware Supreme Court rejected the legitimacy of expert testimony linking the heartburn drug Zantac to cancer, in a major win for makers of the product.

The US Food and Drug Administration has started making rejection letters that pharmaceutical companies traditionally keep under wraps more easily available to investors and the public, a move with the ...

Leading vaccine scientists are calling for more resources to research vaccine safety and support people with claims of injury, and asking HHS Secretary Robert F. Kennedy Jr, who has a history as an ...

Every state has a capitol that houses its state legislature. Many are domed buildings similar to the US Capitol, but others ...

Nearly 81 years to the date after 20-year-old Army Pfc. John L. Moore was wounded while fighting to liberate Europe during WWII, the Purple Heart he earned that day is now in the hands of his only ...

clearance from the U.S. Food and Drug Administration (FDA) for AISight® Dx*—its digital pathology image management system—for use in primary diagnosis in clinical settings. Building on the initial 510 ...

Gov. JB Pritzker will announce this morning that he will seek a third term next year, answering a question about his immediate political future but leaving unanswered whether he will pursue a ...

We can't stand by while Washington plays politics with our health, our future, and our hardest-working families.

Cellectar Biosciences Submits Phase 1b Clinical Trial Protocol to US Food and Drug Administration for CLR 125 to Treat Triple-Negative Breast Cancer (TNBC) ...

U.S. Food & Drug Administration (FDA) Approves Investigational New Drug (IND) Application for Myrio's Lead Product (PHOX2B PC-CAR T) for the Treatment of Neuroblastoma By Myrio Therapeutics ...

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.