FDA clarifies its regulatory to do list for medical devices in 2017 from big data to cybersecurity

Sep 22

Clinical trial design. Cybersecurity. Big data. Those are a some of the 10 items on the U.S. Food and Drug Administration’s list of regulatory science priorities for medical devices in 2017, highlighted in a new report by the Center for Devices and Radiological Health.

Here are a some of the most interesting ones highlighted below:

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