In October 2024, the U.S. Food and Drug Administration (FDA) approved SELARSDI™for all indicationsmatching the reference product ...
The Food and Drug Administration (FDA) and Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) met on Tuesday to optimize the facilitated review pathway (FRP) to expedite access to essential ...
In addition to AVT06, which is a biosimilar candidate for Eylea ® (aflibercept) 2 mg, Alvotech is currently also developing AVT29, a biosimilar candidate for Eylea ® HD (aflibercept) 8 mg. Teva also ...
At least 20 staffers reviewing Neuralink, Elon Musk's brain implant company, were fired in an ongoing DOGE purge of federal workers.
Explaining America’s weirdly complicated food inspection system, including who regulates poultry and eggs and how Robert F.
Tobacco harm reduction advocates in the Philippines lauded the U.S. Food and Drug Administration’s marketing authorizations ...
Sotagliflozin, a drug recently approved by the Food and Drug Administration to treat type 2 diabetes and kidney disease with additional cardiovascular risk factors, can significantly reduce heart ...
according to the Food and Drug Administration — and that percentage is expected to grow. The United States has also operated in an “agricultural trade deficit,” which means that it has ...
Ozempic is a solution for subcutaneous injection that’s approved by the Food and Drug Administration (FDA) to: An interaction occurs when one substance causes another substance to have a ...
such as the Food and Drug Administration (FDA), maintain their authority to ensure these products meet high safety standards that protect children from potential harm. The Philippines faces a ...
I explained why this armchair assessment is wrongheaded, and the security threats Trump’s administration has already left Americans vulnerable to through its actions just one week into his term.
has now also been approved by the US Food and Drug Administration to reduce certain risks associated with chronic kidney disease, drugmaker Novo Nordisk said Tuesday. A Phase 3 clinical trial ...
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