Pharma & Biotechlongitudinal monitoring and comparative effectiveness analysisemerging but credible; enabled by a formal fda program running through fiscal years 2023-2027.

AI-assisted post-approval evidence generation using real-world data

After a drug is approved, companies may still need more proof. Real-world patient records can be organized and analyzed to meet those follow-up requirements, with FDA discussing the plan early.

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Executive Brief

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Value Drivers

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Key Competitors

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