But the Trump administration’s cuts to HIV programs in the U.S. and abroad could undermine the drug’s rollout.

The approval could slow new infections and move the world closer to eliminating HIV. But huge obstacles remain.

HADLIMA™ (adalimumab-bwwd) injection, 40 mg/0.4 mL & 40 mg/0.8 mL is now interchangeable with all high- and low-concentration presentations (autoinjector, prefilled syringe, and single-dose vial ...

Filipinos can now grill authentic samgyeopsal (pork belly strips) from South Korea. After six years, the Food and Drug ...

Dr. Martin Makary is the Commissioner of the Food and Drug Administration (FDA). Relevant to this discussion is this academic paper published by RealClearJournals’ Journal of the Academy of ...

The Food and Drug Administration is drawing ... in how food inspections are done by the FDA would take significant time and resources. "So far, this Administration has acted with reckless ...

MOLBREEVI in autoimmune PAP has been granted Fast Track and Breakthrough Therapy Designations by the FDA, Orphan Drug Designation by the FDA and the European Medicines Agency (EMA), as well as ...

Savara Receives Refusal to File (RTF) Letter From the U.S. Food and Drug Administration (FDA) for the Biologics License Application (BLA) for MOLBREEVI* to Treat Patients With Autoimmune Pulmonary ...

Experts have urged the Philippine government to expedite the approval of a new-generation of dengue vaccine, amid the rising ...

Tubs of pistachio cream are being recalled after nearly half a dozen people reported becoming ill with salmonella infections in the United States, according to the U.S. Food and Drug Administration ...

The U.S. Food and Drug Administration plans to require new clinical ... adults and those at risk of developing severe illness, FDA leaders said on Tuesday. FDA Commissioner Marty Makary and ...