The U.S. Food and Drug Administration on Jan. 6 issued new draft guidance to help improve the accuracy and performance of pulse oximeters that are used for medical purposes across populations with a r ...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 ...
At a CVS store in a racially diverse neighborhood in Brooklyn Center, the only devices available to shoppers to measure their ...
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The FDA has shared draft guidance on the design and development of AI-enabled medical devices and marketing submissions for those devices.
The FDA has released draft guidance for developers of AI-enabled medical devices, offering recommendations aimed at ensuring the safety and effectiveness of the devices.
The Food and Drug Administration issued draft guidance Jan. 6 on marketing submissions and lifecycle management for ...
The FDA does not favor commonly used descriptors such as ‘plant-based burger' on labels and suggests brands instead say ...
The US Food and Drug Administration has issued guidance urging sponsors and trial sites to consider the necessity of the ...
Comment period is open for the public to review the new draft guidelines for labeling plant-based alternative foods.
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