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From speeding up clinical trials to better pre and post market
pharmacovigilence, life sciences organizations can benefit immensely from
safety analytics solutions. But, safety database solutions focused solely on
collecting and reporting company product ADR events do not offer the
functional breadth and depth needed to offer these benefits. A truly effective
safety analytics system must be
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Capable of integrating much more data from diverse internal and external
sources.
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Capable of keeping event and medication data consistently coded at speeds consistent with intended use.
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Provide features for configurable aggregation of data at multiple levels.
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Provide features for specifying when and how alerts are to be generated based
on data.
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