PPD Blog
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

Shefali Shah, principal of market access consulting, Evidera, and John Rafa, senior director of market intelligence, Accelerated Enrollment Solutions (AES), 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.



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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