Featured Articles
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Helping To Power The WHO Solidarity Trial Against COVID-19
3/21/2025
To overcome the unprecedented challenges of large-scale global clinical trials, adopting data capture solutions is essential for ensuring the success of critical research initiatives.
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The Catch-22 Of eConsent: A Missed Opportunity For Improved Trials
3/21/2025
Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.
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Strategies To Minimize Participant And Healthcare Provider Burden
3/21/2025
Patient-reported outcomes (PROs) are vital for clinical trials but can burden participants and providers. Discover strategies and practical solutions to ease these burdens and improve data quality.
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Do CROs Need To Reinvent Themselves In 2025?
3/21/2025
Facing economic pressures, regulatory changes, and technological advancements, learn why CROs must redefine their value propositions and discuss the need for reinvention in 2025.
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Build Vs. Buy Vs. Partner In Life Sciences: Making The Right Call
3/21/2025
Discover when life sciences organizations should develop technology in-house, buy off-the-shelf solutions, or form strategic partnerships as well as explore the costs, risks, and trade-offs that come with each approach.
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Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study
12/20/2024
This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.
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eCOA Evolution: Have We Overcomplicated It?
11/21/2024
eCOA has evolved from simple data collection to complex patient engagement platforms, raising concerns about added complexity. Explore innovative tools aimed at simplifying this complexity.
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Waiver Of Consent vs Waiver Of Written Consent
11/21/2024
Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.
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5 Best Practices For Getting Started With ePRO
9/16/2024
Unlock the potential of electronic Patient Reported Outcomes (ePRO) in your clinical research by implementing these essential best practices for success.
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Understanding Phase 4 Trials: A Critical Component Of Post-Marketing Insight
9/16/2024
Uncover how Phase 4 trials play an essential role in gathering additional real-world data on the treatment’s performance over a longer period of time and in more diverse patient populations.