CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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What Sites Wish Tech Vendors (And Sponsors) Heard At SCDM But Probably Didn't
During a Society for Clinical Data Management (SCDM) panel discussion, three site-side representatives discussed the challenges clinical research coordinators have executing their clinical duties amid increasingly complex data entry demands.
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SCDM 2025: Practical Advice From Global Regulators — Including The FDA
Discover what regulators from around the world, including the FDA, think should be top of mind for clinical data managers.
ECOA RESOURCES
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Learn how the built-in flexibility and freedom of eCOAs can enhance many aspects of a clinical trial.
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From eRecruitment, pre-screening, eConsent, and image-based data capture, explore how a decentralized trial design helps streamline enrollment, increase patient retention, and ensure data quality.
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Greta van Schoor attended the 31st Annual ISOQOL Conference, where HRQOL leaders shared insights on optimizing eCOA collection, integrating PROs, and digital health in clinical research.
ECONSENT RESOURCES
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The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.
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Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.
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In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.
EPRO RESOURCES
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Explore the importance of involving caregivers in the care process and how electronic patient-reported outcomes technology can facilitate communication, tracking, and collaboration.
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Greta van Schoor attended the 31st Annual ISOQOL Conference, where HRQOL leaders shared insights on optimizing eCOA collection, integrating PROs, and digital health in clinical research.
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See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.