The US Food and Drug Administration (FDA) has approved the abbreviated new drug application (ANDA) of Lupin’s Sacubitril and ...

The expanded indication allows esketamine nasal spray to be used as a standalone treatment in adults with MDD who have not ...

The FDA rejected the company’s initial NDA in 2021, citing the lack of an adequate trial to demonstrate efficacy.

Explaining the decision to re-employ the current drug controller general of India, the health ministry has told the ...

Liability and injury: Changes to the existing liability protections for certain vaccine makers and modifications to the list ...

X4 Pharmaceuticals (Nasdaq: XFOR), a company driven to improve the lives of people with rare diseases of the immune system, today announced that its Marketing Authorization Application (MAA) for ...

Clarity Pharmaceuticals (ASX: CU6) ("Clarity" or "Company"), a clinical-stage radiopharmaceutical company with a mission to ...

In the field of biomedical nanotechnology, chitosan and alginate —both naturally derived biopolymers — have garnered significant attention due to their ...

President Donald Trump has been urged by a conservative think tank to release Prince Harry’s immigration files, alleging that ...

The Food and Drug Administration, a federal agency of the HHS, usually releases updates on probes of outbreaks linked to ...

The Department of Justice says it will "vigorously defend" Donald Trump's executive order ending birthright citizenship, after it was temporarily blocked in a federal court earlier today.

His team at HHS has paused critical communications and meetings, right as public health officials are worried about bird flu.