mHealth Innovation_Identifying the Best Patient-Centered Tech for Clinical Trials
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This whitepaper discusses the changes in master protocols within the clinical research community and walks through best practices on how to address the changes.
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In this article Angela Qu, M.D., Ph.D., Vice President, Biomarkers and Genomic Medicine, discusses the pan-cancer drug development approach guided by biomarkers.
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This article discusses the increasing use of AI in pharmacovigilance activities to increase efficiency and outcomes as data volume continues to increase.
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Learn how all stakeholders benefit when patients and their insights are at the heart of every aspect of clinical development.
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Decentralized clinical trials, where portions of a study are conducted outside a traditional trial site, offer new opportunities — and new hope — for patients struggling with inflammatory conditions.
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Expert perspectives from Parexel's Leanne Larson, Senior Vice President and WW Head of Real-World Evidence
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This article explores the nature and manufacturing process of ATMP and how clinical professionals can execute the development and marketing of these therapies.
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This article provides insight into how clinical research organizations can carefully create robust planning and optimization solutions with IDMP integrity in mind.
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There are challenges at every point in the clinical supply chain process. This article reviews the risks associated with the planning and execution of a clinical site supply strategy.
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Learn how Parexel accelerates clinical development through enhanced biologic management—and our steps in supporting our clients and patients along the way.
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What the industry is currently experiencing is an evolution of processes founded in solid science and good clinical study practices.
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In this article, we summarize what we’ve learned and outline the top 10 rules for a successful DCT.
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