Years of research have showed that pulse oximeters yield less accurate readings for people with darker skin tones, and now ...
New draft guidelines would increase the number of people with darker skin who should be included in clinical trials of the ...
KTVZ News has an update Friday on our previous reports about the sometimes tragic results from use of Librela, a once-monthly ...
Bryan Johnson, a tech entrepreneur, has stopped using rapamycin, a drug not approved for anti-aging by the FDA, following ...
The agency is proposing that device manufacturers improve their testing to including larger, more diverse sample sizes.
The FDA's draft recommendations for pulse oximeters aims to include clinical studies involving at least 150 participants with ...
Rather than relying on those testing the devices to judge skin tones, the draft guidance suggests manufacturers should use ...
Federal health officials are proposing changes to make sure medical devices that measure oxygen levels are working for ...
Dr. Eric K. Singhi discusses the significance of the FDA approval of subcutaneous Opdivo for patients with solid tumors.
The U.S. health regulator on Monday proposed a new guidance for widely used blood oxygen monitoring devices to improve their ...
The US Food and Drug Administration has issued guidance urging sponsors and trial sites to consider the necessity of the invasive procedure and gaining assent and consent from children ahead of trials ...
The U.S. Food and Drug Administration proposed new guidance for devices used to monitor blood oxygen levels to improve their ...