Manufacturers increasingly but still infrequently follow Food and Drug Administration guidance that recommends testing pulse oximeters on participants with a range of skin pigmentations, according to ...
NIST added that the public input on the guidance, titled Recommendations for Key Encapsulation Mechanisms, will help it ...
4hon MSN
At a CVS store in a racially diverse neighborhood in Brooklyn Center, the only devices available to shoppers to measure their ...
On January 6, the FDA announced the availability of draft guidance on accelerated approval for drugs and biological products, and consideration ...
The Federal Housing Administration has released its first non-draft update of guidance on which defects it's most concerned about and what to do about them.
The U.S. Food and Drug Administration on Jan. 6 issued new draft guidance to help improve the accuracy and performance of pulse oximeters that are used for medical purposes across populations with a r ...
The Virginia Department of Education is hosting a public comment meeting on Thursday, January 9, at 5:30 p.m. on its draft to ...
FDA published a draft guidance titled Establishing Sanitation Programs for Low-Moisture Ready-to-Eat Human Foods and Taking ...
An advisory panel, formed under the IndiaAI Mission, has suggested sweeping reforms to the regulatory landscape to govern AI ...
The Food and Drug Administration on Monday issued a guidance for the tobacco industry entitled Validation and Verification of ...
The agency is proposing that device manufacturers improve their testing to including larger, more diverse sample sizes.
The FDA has shared draft guidance on the design and development of AI-enabled medical devices and marketing submissions for those devices.
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