PPD brings extensive experience in the nuances of post-approval studies, combined with a solid foundation in late-stage clinical trials management.
PPD’s endocrinology and metabolic clinical trial experience helps us to manage programs of any size and complexity around the world.
As clinical trial investigators, physicians play an integral role in the development of life-changing medicines.
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How data-driven solutions help us focus on our patients
Jolee Graham, biostatistics director, Nicki Payne, director, IRT, and Katy Tam, director, biostatistics, discuss the components of successful randomization in research.
An overview of anonymization strategy for clinical documents in response to EMA Policy 0043 and Policy 0070
Philip Bartle, an associate director in clinical innovation, discusses the use of industry data standards, which can greatly drive efficiencies and reduce variations in data.
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