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What’s best way of regulating digital health software as medical device? FDA seeks answers with pre-certification program

18:15 EDT 28 Jul 2017 | MedCity News

Pros and cons empty list on blackboard

The FDA is seeking nine companies for a pilot of its pre-certification program accepting applications from companies developing digital health software as a medical device set to kick off September 1.

Original Article: What’s best way of regulating digital health software as medical device? FDA seeks answers with pre-certification program

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