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23/03/2013Five things we learned from the FDA’s medical app testimony | mobihealthnews
This morning the FDA’s Christy Foreman, who serves as the Director of the Office of Device Evaluation at the Center for Devices and Radiological Health, shared a number of insights about mobile medical app regulation that before today had not been revealed. Here are five things we learned from the FDA’s testimony during the congressional hearing today…
See on mobihealthnews.com
