Which government agency issues guidelines on the regulation of medical apps for mobile phones?

The Food and Drug Administration (FDA) is the government agency responsible for issuing guidelines on the regulation of medical apps for mobile phones. This agency oversees the safety and efficacy of a wide range of medical products, including digital health tools. The FDA has established a framework to ensure that mobile medical applications are safe to use and perform their intended functions effectively, protecting users from potential risks associated with these technologies. This regulatory oversight is particularly important as digital health solutions become increasingly prevalent in healthcare, ultimately aiming to improve patient outcomes and ensure public health safety.

The other options mentioned do not focus on the regulation of medical apps: Health and Human Services primarily oversees public health policies; the Federal Bureau of Investigation is focused on law enforcement and national security; and Homeland Security deals with domestic security issues and emergencies, rather than health technology regulation.