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SCOPE 365 is the year-round digital extension of SCOPE, bringing clinical research professionals continuous access to insights, live virtual meetups, expert interviews, and premium intelligence products. It’s a centralized hub designed to help sponsors, CROs, sites, and solution providers stay on the pulse of the industry, elevate thought leadership, and maintain momentum between SCOPE’s global conferences.

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  • Reverse Translation: Why Completed Trials Should Inform Future Design

    We all know, clinical research generates enormous volumes of data. And these volumes continue to grow. Every completed study contains detailed information on endpoints, eligibility criteria, enrollment performance, adverse events, dosing strategies, and operational outcomes. Yet once a trial closes and regulatory submissions are complete, much of that data becomes archival. It sits in repositories. It is referenced occasionally. It is rarely treated as an active design asset. This is beginning to change. Reverse translation, the practice of feeding insights from completed clinical trials back into earlier stages of development, offers a powerful opportunity to improve future study design.

    Mar 31, 2026

  • Long Screening Visits, Short Patience: Rethinking the Study Start Experience

    The first study visit sets the tone for everything that follows. For patients, screening is their introduction to clinical research. It is where expectations are formed, trust is built, and burden becomes real. For sites, it is often one of the most resource-intensive moments in the trial lifecycle. Yet screening visits have steadily grown longer and more complex. Additional laboratory panels, imaging requirements, multiple questionnaires, device training sessions, and layered consent discussions can turn what was once a straightforward evaluation into a multi-hour commitment. In some studies, screening stretches across multiple visits over several weeks. The impact is rarely neutral.

    Mar 26, 2026

  • Disease Progression Modeling: When to Use It — and When Not To

    Model-informed approaches are gaining traction across clinical development. Among them, disease progression modeling has attracted increasing attention. When applied thoughtfully, it can help sponsors design more efficient trials, select more sensitive endpoints, and make better-informed go or no-go decisions. But like any tool, disease progression modeling works best when used for the right questions. Understanding when to use it, and when it adds limited value, is critical.

    Mar 24, 2026

  • Measuring What Matters: The Case for Standardized Patient Feedback in Clinical Trials

    We track biomarkers with precision. We analyze endpoints with statistical rigor. We monitor safety signals in real time. Yet when it comes to measuring the patient experience of participating in a trial, the approach is often informal, inconsistent, or reactive. That gap is becoming harder to justify. If patient centricity is a serious goal in modern clinical development, then patient feedback must be measured with the same discipline applied to clinical endpoints.

    Mar 19, 2026

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What You’ll Find in SCOPE 365

SCOPE of Things Podcast

SCOPE of Things

The Scope of Things podcast explores clinical research and its possibilities, promise, and pitfalls. Clinical Research News Senior Writer, Deborah Borfitz, welcomes guests in the field.
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Voices of SCOPE

Voices of SCOPE

Voices of SCOPE brings you unfiltered conversations with the people driving change in clinical research. These straight-talk interviews spotlight real lessons, fresh ideas, and practical innovations from leaders across pharma, biotech, tech, and patient advocacy.
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SCOPE Summaries

SCOPE Summaries

Concise, accurate summaries of key presentations from SCOPE Summit U.S., SCOPE Europe, and SCOPE X, designed to help you quickly absorb what matters most.
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