CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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From 73% Noncompliant To 2.4%: Building A Compliance Office
How one research administrator cut a university's clinical trial disclosure noncompliance from 73% to 2.4% in two years, then built a second office.
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A Framework For Diagnosing Clinical Research Technology Maturity
A 30-year clinical research veteran breaks down the four stages of technology maturity and why most organizations misjudge their own.
ECOA RESOURCES
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In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.
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Whether you're looking for no-code simplicity, low-code adaptability, or fully programmable control, this purpose-built technology platform supports trials of all complexities with ease.
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TransPerfect Life Sciences' C3 Summit brings to you virtual sessions on how the paper to digital migration is evolving, the use and application of eCOA migration technology, and setting up successful eCOA solutions.
ECONSENT RESOURCES
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Discover how digital consent is working to enhance diversity, empower participants with education, drive quality data, and streamline operations.
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A top-10 pharmaceutical company was looking to reduce the amount of administrative burden on their clinical trial sites and themselves. See how we accomplished it, using eConsent.
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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.
EPRO RESOURCES
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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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Dive into the prediction that the rapid adoption of eCOAs will continue to grow in 2022, as sponsors acknowledge how useful these tools have become in decentralized clinical trial (DCT) settings.
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PRO and COA strategy is now central to trial success. Organizations that capture meaningful patient experience data will gain stronger evidence and a regulatory advantage.