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Browse our Biotech resources to find the latest articles, blogs, brochures, and videos from our experts. See the latest content below.
Lucas Kempf, former regulator, reflects on his time at the FDA and outlines why companies should invest in a high-quality natural history study.
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This article summarizes a recent panel discussion where experts from Parexel and biotech company, MorphoSys, shared their experiences from recent pioneering efforts in RWE.
New ways of thinking are needed about vast sources of data amassed — and how that data can be fit-for-purpose to meet drug approval and access standards.
Parexel Biotech has created this guide to simplify the nomenclature and types of real-world studies.
Expert perspectives from Parexel's Leanne Larson, Senior Vice President and WW Head of Real-World Evidence
We have created this guide to simplify the terminology of real-world evidence (RWE) and outline some of the strategic options available.
Parexel's Amy McKee and Leanne Larson make a case for an evidence-driven approach to drug development.
What the industry is currently experiencing is an evolution of processes founded in solid science and good clinical study practices.
Matthew Gordon, VP of Real-World Evidence Strategy, Parexel, and Jimmy Brown, VP, Parexel Biotech discuss how RWE is a tremendously versatile tool for biotech companies at all stages.
Parexel’s Leanne Larson, Corporate VP and WW Head, Real-world Evidence speaks with Deborah Collyar, cancer survivor and President of Advocates in Research about the importance of Real-world Evidence
How China and Japan are approaching early challenges in using real-world evidence.
The UK national health technology assessment (HTA) body, the National Institute for Health and Clinical Excellence (NICE), made a long-awaited announcement last week: NICE has expanded the...
Let us show you how our experience of leveraging real-world data (RWD) and real-world evidence (RWE) can help your product launch succeed.
Parexel offers a complimentary, educational workshop custom built to your evidence and market access needs.