“The FDA's filing acceptance of Dr. Reddy's proposed denosumab biosimilar marks an important milestone in bringing this biosimilar medication to more patients throughout the U.S.,” said Milan ...

With ketamine removed from the FDA drug shortage list, the FDA is expected to restrict ... solicitation or sale would be unlawful prior to registration or qualification under the securities laws of ...

Journal of the American Medical Association study provides further evidence that Multikine can treat unmet need in ~70% of ...

Dr. Reddy’s Laboratories RDY and partner, Alvotech ALVO, announced the FDA’s acceptance of a regulatory filing, seeking the ...

The 6-month room temperature stability on this batch adds to the nine-month data accumulated on a previous batch produced by ...

The Food and Drugs Authority (FDA) has responded to a recent BBC Africa ... Additionally, the FDA has suspended the processing of product registration applications from Masters Pharmaceutical ...

In a significant crackdown on illicit drug smuggling, the Keta Divisional Police Command in the Volta Region have arrested ...

Additionally, the Maharashtra FDA issued a Stop Production Order on February 22, 2025, halting the manufacturing of the illicit drug combinations ... either a Product Registration Certificate ...

Lacutamab is granted European Medicines Agency (EMA) PRIME designation and US Food and Drug Administration (FDA) granted Fast Track designation ... The Sézary syndrome cohort of the study could enable ...

The Traditional Herbalist Association Ghana (THAG) has urged the government to invest in traditional and herbal medicine to ...

Registration and reporting of clinical trial results required by FDA regulations Some studies are required to be registered at ClinicalTrials.gov in accordance with the federal regulations in Section ...