Are you ready to launch your mobile medical app in the United States? Depending on the functionality of your app, you might need clearance from the US Food and Drug Administration. But with thousands of apps on the market, how do you know if yours requires FDA clearance?
Mobile medical applications are moving targets as far as the FDA is concerned. While some requirements are well-defined, the FDA still reserves the right to regulate any mobile medical device on an individual basis. As a result, medical app developers face a very difficult task when it comes to determining how FDA regulations apply to their product. In this white paper (English only), we will address your biggest questions about mobile medical app regulations in the US market.
What you will learn in this 7-page white paper:
We answer all of these questions and many more in this whitepaper (English only).
Ready to sell your medical device in the United States? The first step is to classify your device according to the US FDA classification system. An
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