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As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its ...
U.S. FDA issues Form 483 with 2 observations to Dr. Reddy's Laboratories' API manufacturing facility in Miryalaguda.
Dr Reddys Laboratories said that the United States Food & Drug Administration (US FDA), post a GMP inspection, has issued a Form 483 with 2 observations to the company's Telangana-based manufacturing ...
In calling for more clinical testing of vaccines in younger people and those who face a low risk of severe disease from Covid ...
Susvimo is the first and only FDA-approved, continuous delivery treatment shown to maintain vision in people with DR with ...
Merck beats Q1 2025 estimates despite Gardasil sales drop, driven by Vaxneuvance, Winrevair & Welireg. Click here to find out ...
Hyderabad: Dr Reddy's Labs has announced that the United States Food & Drug Administration (USFDA) has issued two ...
The Food and Drug Administration (FDA) has approved Susvimo ® (ranibizumab injection) for the treatment of patients with ...
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