A Democratic lawmaker is raising new concerns about a Food and Drug Administration program designed to drastically shorten ...
Trump administration officials vetoed the FDA's plan to fast-track the review of a psychedelic treatment for severe ...
At an employee town hall, FDA leaders tried to quell staff concerns about a controversial new program to fast-track certain drugs.
Feb 3 () - AstraZeneca said on Tuesday the U. health regulator has rejected its application for a self-injectable version ...
Feb 4 (Reuters) - Medical device maker Abbott Laboratories has reported 860 serious injuries linked to the recall of some of its glucose monitoring sensors, the U.S. Food and Drug Administration said ...
Let’s be clear: 7-OH is not a public health crisis. According to the Food and Drug Administration’s (FDA) own Adverse Event Reporting System (FAERS), and shown in the Marwood Report, there have been ...
Feb 4 (Reuters) - The U.S. Food and Drug Administration on Wednesday classified Abbott's recall of certain glucose monitoring sensors as the most serious after reports tied the devices to seven deaths ...
The Food and Drug Administration indicated that a "floating black foreign substance in the product" precipitated the multistate recall, but the agency neither identified the material nor provided any ...
The US health department’s inspector general is investigating whether a top US Food and Drug Administration official misled the federal government by using a sham divorce to avoid running afoul of ...
A supplement advertised as a honey product used for energy support has been recalled because it contains a drug that users aren’t aware of. Ashfiat Alharamain Energy Support was distributed nationwide ...
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