Tag Archives: FDA
Mobile medical apps: lobbying in the USA
The FDA is the responsible organisation for the regulation of medical devices in the USA. In a proactive move, the FDA published draft guidance (21 July 2011) for what it defined as “mobile medical applications”, and invited comments from industry … Continue reading →
Posted in News, Policy
|
Tagged apps, FDA, FDASIA, health apps, Health IT, Lobbying, mHealth, regulation
|
Leave a comment