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Pharma Execs Prefer Hybrid Clinical Trials
Author: Darcy Forman, Chief Delivery Officer Decentralized clinical trial methods are being adopted at a […]
BLOG
A Long-Time Pharmaceutical Executive’s Experience Participating in a Clinical Trial
With 15 years of experience in pharmaceuticals, Science 37’s Leah Zilla thought she knew what to expect […]
BLOG
Decentralized Clinical Trials—Where the Industry is Now
Author; Darcy Forman, Chief Delivery Officer The widespread adoption of telemedicine ushered in by the […]
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How to Operationalize Infectious Disease Trials with a Virtual Site
Download our Infectious Disease Clinical Trial Playbook to discover the premier, patient-centric strategy for solving […]
Clinical Decision Makers Confirm a Shift to Hybrid and Decentralized Studies
Clinical research is undergoing transformation across the board—but how will it impact oncology clinical trials? […]
whitepaper
Decentralized Clinical Trials — Is There a Positive Return on Investment on a Virtual Site?
Across the Life Sciences industry, there has been much talk about the cost and value […]
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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.
on demand webinar
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.
on demand webinar
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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