The Department of Agriculture (DA) and the Food and Drug Administration (FDA) are strengthening their collaboration on ...

Both the U.S. Food and Drug Administration (FDA ... including the evaluation of events with high background rates, long latency periods, or a possible contribution by the disease itself.

As a Dresden International University-trained preventive medicine and dermatology specialist practicing in Metro Manila, I’ve witnessed firsthand how ...

White House press secretary Karoline Leavitt delivered a tirade Thursday against a federal judge who ruled against Donald ...

The FDA is likely to approve the first treatment for smoldering multiple myeloma but pass on a new option relapsed/refractory DLBCL, after votes by its Oncologic Drugs Advisory Committee.

Samsung Biologics spins off Samsung Bioepis Holdings to enhance competitiveness Samsung Bioepis Holdings aims to streamline ...

A new government-issued report reflects some of the most controversial views on vaccines, the nation’s food supply, ...

Discover how ReviTag's natural blend of collagen-untangling ingredients targets skin tags and boosts skin clarity-backed by ...

Investigator-initiated Phase 2 trial to evaluate TNX-102 SL's potential to reduce severity of acute stress reaction (ASR) and ...

Mounjaro was approved by the Food and Drug Administration (FDA ... For instance, patients may already be on other background drugs being administered as a standard of care. A trial can still ...

US Health and Human Services Robert F. Kennedy Jr. announced Tuesday said the Covid-19 vaccine will no longer be among the recommended vaccines for pregnant women and healthy children on the US ...

Commission, as established by President Donald Trump's Feb. 13, 2025, Executive Order (EO) 14212, released its inaugural report on May 22, 2025, titled "The MAHA Report: Making Our Children Healthy ...