The Food and Drug Administration April 29 issued a final rule that would phase out its general enforcement discretion ...
The Food and Drug Administration (FDA) is revising long-standing rules to place laboratory tests under the same jurisdiction ...
Dublin, Ohio-based Cardinal Health was found to be marketing convenience kits containing certain piston syringes manufactured ...
The U.S. Food and Drug Administration (FDA) on Monday tightened regulations for clinical laboratories with a new rule that ...
The FDA has finalized its regulatory rule that aims to bring laboratory-developed tests more in-line with how the agency ...
ResMed said that the medical device ... This includes rules to keep the magnets at least six inches from implants or devices ...
When the FDA recently convened a committee of advisers to assess a cardiac device made by Abbott, the agency didn’t disclose ...
said Sanket Dhruva, a cardiologist and an expert in medical device safety and regulation at the University of California-San Francisco. Though some surgeons may have been aware of issues ...
When the FDA recently convened a committee of advisers to assess a cardiac device made by Abbott ... s approach to disclosure ...
When the Food and Drug Administration recently convened a committee of advisers to assess a cardiac device ... with rules for conferences at which doctors earn credit for continuing medical ...
When the FDA recently convened a committee of advisers to assess a cardiac device made ... contrasts with rules for conferences at which doctors earn credit for continuing medical education.