A new rule has been recommended in the Federal Register, which would change mobile health technology classifications. The Food and Drug Administration has now proposed a new rule within the Federal Register which would make changes to the way that it would classify mhealth devices, which could be quite beneficial to that industry. The proposed rule would make it easier for the agency to classify a mobile medical device. Should this become the rule, it will be simpler for the FDA to be able to classify mhealth devices under 2012’s…
Read MoreMhealth to benefit from newly proposed FDA regulations
