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Decentralized Clinical Trials: Why They Matter

Author: Darcy Forman, Chief Delivery Officer, Science 37 In the past few years, the clinical […]

The Time for Decentralized Clinical Trials is Now

The FDA Draft Guidance on Decentralized Clinical Trials provides recommendations for clinical trial sponsors to […]

Three Ways the Metasite™ Model Creates Value for Dermatologic Clinical Trials

Author: Robert Stavert, M.D., M.B.A, Medical Director, Dermatology, Science 37 The past decade has brought […]

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Reports & White Papers

New FDA Draft Guidance Shows That the Time for Decentralized Clinical Trials is Now

On May 1, 2023, the U.S. Food and Drug Administration (FDA) released an updated Draft Guidance on […]

Transform Observational Studies with a Virtual Site

Are your observational or long-term follow-up studies facing challenges? Are keeping protocols open across multiple […]

How to Save an At-Risk Clinical Trial

How can you rescue an at-risk clinical trial without compromising quality? Delays in clinical research […]

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Webinars

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Disrupting the Clinical Trial: When to Decentralize?

Learn more about agile technologies and industry standards that are needed to drive clinical trial innovation, as we move towards universal adoption of decentralization.

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Virtual Sites - Are They the Future of RWE?

The adoption of virtual sites, that are powered by decentralized clinical trial tools, has increased exponentially in recent years. In this video-on-demand, industry leaders discuss how virtual sites can be implemented to improve real-world data access and long-term follow-up, as well as elaborate on the value virtual sites deliver to patients, sponsors, and CROs alike. Learn how virtual site elements are incorporated today, and how the landscape will change in the years to come.

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Let's Plan, Do, Check, and Act: Leading Diversity in Clinical Trials Through Effective Metrics

The Equity intention of the FDA is clear, the pharmaceutical industry must provide a Diversity Action Plan for all submissions—making trials more inclusive. This must be done through an evidence-based approach, providing a rationale for efficacy and safety to underrepresented populations, describing how the trials address inclusion, establishing goals for enrollment, operational tactics for enrollment and retention, and continuous monitoring to improve plans.

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Podcast & Other Media

AWS Health Innovation Podcast: Accelerating Clinical Trials & Making Research More Accessible

Darcy Forman, Chief Delivery Officer at Science 37, joins Alex Merwin at AWS to talk about Science 37’s trailblazing role in evolving how clinical research is conducted.

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