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PPD Blog

Sharing industry knowledge as we
help deliver life-changing therapies.

 

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Reinforcing a Shared Mindset with Our Clients at PPD Biotech University

Elisha Talley-Roithner, global head of operations, PPD Biotech, discusses PPD Biotech’s Biotech University and its unique training capabilities.

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Why Payer Perspectives Should Be on Your Radar Now–Even if Your Launch is Years Away

Our experts write about payer/health technology perspectives and trial design, optimal approaches for incorporating feedback and more.

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The Benefit of Registries for Real-World Evidence Generation in Rare Disease Research

Linda Ross, senior director, peri- and post-approval operations, Evidera, discusses how registries can be an incredibly useful tool in research.

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Infrastructure Design: Key to Enhanced Clinical Trials Data Management

PPD Laboratories experts on PPD's central lab data management service and how it can mitigate challenges throughout a trial.

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Natural History Studies in Rare Diseases and Genetic Biomarkers

By Andrew Bevan, director, project management, peri- and post-approval operations, Evidera; Moira Ringo, senior consultant, real-world evidence, Evidera; Leona C. Fitzgerald, senior director, regulatory affairs, PPD; Fiona Kearney, senior director, project management, peri- and post-approval operations, Evidera; and Delphine Saragoussi, research scientist, real-world evidence, Evidera.

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