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FDA Audits Pulse Oximeter Efficacy To Address Digital Health Bias

Food and Drug Administration FDA to schedule public meeting of Medical Devices Advisory Committee to discuss study results about pulse oximeter performance. Meeting consistent with agency efforts to evaluate clinical trial design transparency, diversity, AI development need. ....

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FDA Audits Pulse Oximeter Efficacy To Address Digital Health Bias

FDA Audits Pulse Oximeter Efficacy To Address Digital Health Bias
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Michael Sjoding , Drug Administration , Devices Advisory Committee , Medical Devices Advisory Committee , Medical Devices Workshop , New England Journal , Diversity Plans , Improve Enrollment , Participants From Underrepresented Racial , Ethnic Populations , Clinical Trials , Clinical Trial Populations , Eligibility Criteria , Enrollment Practices , Trial Designs ,

Doctors Still Overprescribing Fluoroquinolones Despite Risks

Since the 1980s, more than 60,000 patients have reported hundreds of thousands of serious events linked to fluoroquinolones to the FDA, including 6575 reports of deaths. ....

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Pulse oximeters missed low oxygen levels in more Black veterans than White veterans

Pulse oximeters missed low oxygen levels in more Black veterans than White veterans
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Durbin tallies new youth vaping following FDA's missed deadline- POLITICO

The Biden administration announced plans to propose a rule that would cap the amount of nicotine in finished tobacco products. ....

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