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Embracing Virtual in Psychiatry Research
The field of clinical research has undergone a remarkable transformation in recent years, accelerated by […]
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Rare Disease Research: The Impact of Decentralized Trials
Authors: Jonathan Cotliar, MD and Suzanne Pendl, MD Collectively, rare diseases are not so rare. […]
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How Decentralized Trials Transform Patient Recruitment
Author: Erica Prowisor, Senior Vice President, Patient and Provider Networks, Science 37 In the dynamic […]
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Science 37 Solutions Fact Sheet
Science 37 offers an innovative suite of patient access solutions aligned with the enrollment and […]
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How to Operationalize Neurology Clinical Trials with the Metasite™
With a virtual site, clinical trial sponsors and research organizations can expand access and accelerate recruitment by allowing patients to participate from anywhere, regardless of location.
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A Survey-Based Exploration of Biopharma's Shifting Landscape and the Crucial Role of Direct-to-Patient Trials
In the ever-changing landscape of clinical research, transformation is driven by forces of economic challenges, […]
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Science 37 Launches Infectious Disease Prevention Study in Just 12 Weeks
A biotech sponsor contracted Science 37 to help enroll patients in a global Phase 2/3 registrational study with 95+ sites in 30 countries. Acting as a virtual site, Science 37 worked alongside traditional sites to reach a broader patient population and accelerate time-to-market.
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The Clinical Trial Shift: Sites that Follow the Patient
In this video-on-demand, find out why a patient-centered approach requires both a shift—a mind shift—and a pragmatic, coordinated approach to seeing it through. Science 37 CEO, David Coman, and VP of Internal Medicine, Dr. Debra Weinstein, join a group of leaders from Bayer, Janssen, and Novartis, to discuss what the ideal patient model really is—and how to deliver this patient-first approach.
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Science 37 Accelerates Oncology Clinical Trial Timeline by 3 Years
A biopharma company was investigating how its diagnostic screening technology—a one-time blood sample—performed against the gold-standard cancer screening procedure. The protocol required 25,000 average-risk patients between the ages of 45 and 85 to enroll. The sponsor also looked to include a diverse and representative population in the trial. See how the Science 37 Metasite™ enrolled nearly 50% of the entire study with 24.2% minority representation, enabling recruitment and access across 49 states. This accelerated approach resulted in a more than 3-year reduction of the clinical trial timeline. Submit the form to watch the case study video.
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