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A U.S. senator is asking the FDA how it will enforce regulations on pharmaceutical advertising after it let go of numerous ...
The Food and Drug Administration has identified a Class I recall of certain lots of BD esophagogastric balloon tamponade ...
The U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) plan to phase out all ...
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Teva Pharmaceutical Industries Limited (NYSE:TEVA) announced today that its investigational drug TEV-53408 has received Fast ...
"Expert Panels with the FDA" are a series of roundtable discussions to provide an open public discourse on the latest medical ...
Commissioner Marty Makary said FDA employees are overseeing the use of AI, but questions remain about how the technology will be applied amid staff cuts.
This designation is meaningful as it signifies our continued commitment to making biosimilars more accessible. Both biosimilars and interchangeable biosimilars are highly similar and have no ...
The Food and Drug Administration (FDA) announced Wednesday plans to help states and Indian tribes import cheaper prescription ...
Savara plans to request a Type A meeting with the FDA within the next 30 days. It is currently generating the data requested by the FDA, and expects to resubmit its application in the fourth quarter ...
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Health and Me on MSNNew Mitral Valve Replacement Device Wins FDA ApprovalThe Tendyne system is designated for those who are at high risk for traditional open-heart surgery. It helps with those with ...
The supply of GLP-1 drugs like Ozempic has been increasing, but they’re still expensive for most patients. Here are answers ...
A joint operation conducted by the Food and Drug Administration and Customs and Border Protection resulted in the seizure of ...
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