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Is this limited to pre-licensure safety, or is FDA and NIH interested in systems that might assist post-licensure safety evaluation on various events that occur with medication use?

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Is this limited to pre-licensure safety, or is FDA and NIH interested in systems that might assist post-licensure safety evaluation on various events that occur with medication use?

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The research scope is not limited to pre-licensure activities but post-market safety assessment is also an important area of research.

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