Healthcare Analytics News December 13, 2018
Samara Rosenfeld

A report by the U.S. Food and Drug Administration (FDA) found that the benefits of digital health tools that are not regulated by the agency outweigh the risks.

FDA Commissioner Scott Gottlieb, M.D., said that there are many digital health products that people are using to track their wellness and health information that are not regulated by the agency. The report touches on tools such as e-prescribing software and mindfulness apps.

The FDA looked at information about the non-device software functions and how the functions impact patient safety.

>> READ: FDA Releases New Data Integrity Guidance to Improve Drug Quality

“In general, the FDA’s analysis found more benefits than risks to patient safety and health from the use of these...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Apps, Digital Health, EMR / EHR, FDA, Govt Agencies, Health IT, mHealth, Patient / Consumer, Provider, Regulations, Technology, Wellness
Early tests of H5N1 prevalence in milk suggest U.S. bird flu outbreak in cows is widespread
Bird Flu (H5N1) Explained: Here’s What To Know—And Why Scientists Are Concerned
2023 Had Most Food Recalls Since Start Of COVID-19 Pandemic, Report Finds
Exo adds FDA-cleared AI tools to handheld ultrasound system
Scopio Labs gains De Novo clearance for AI bone marrow analysis software and more FDA clearances

Share This Article