ePRO/eCOA White Papers & Case Studies
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Pioneering The End-To-End Decentralized Trial Experience
4/16/2025
Explore a collaboration between a top 20 pharmaceutical company and Medidata that highlights the potential of DCTs to transform trial execution, offering a replicable model for future research.
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Digital Outcome Measures Approved As Primary Endpoint In Cardiopulmonary Study
4/15/2025
Discover how a clinical development program was saved using objective, continuous digital outcome measures.
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A New Digital Health Solution For Long-Term Cough Monitoring
4/15/2025
Discover how our innovative solution transforms cough measurement — providing accurate, objective insights to enhance treatment, detect exacerbations early, and improve patient outcomes.
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PPD Monitoring Application (MApp): A Flexible Technical Solution
4/15/2025
This dynamic, system-agnostic approach to modernizing clinical trial monitoring supports targeted oversight, as well as sampling at the subject, visit, and form levels.
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Setting A New Client Standard In Study Closeout Timelines
4/4/2025
Learn how a top-10 global pharmaceutical company achieved a significantly faster time to market for a high-profile therapy.
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6 Key Ways Real-World Data Is Advancing Colorectal Cancer Therapies
4/3/2025
Real-world data (RWD) is transforming Colorectal cancer (CRC) research by complementing traditional clinical trials, accelerating drug development, and improving patient outcomes.
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Timely Lab Data To Inform Outreach To Healthcare Professionals
4/3/2025
Learn how you can leverage a system that offers flexible data delivery formats and seamless integration into commercialization workflows while also ensuring HIPAA-compliant deidentified data for patient privacy.
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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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Hybrid eConsent: Remote And On-Site
3/21/2025
Studies show when participants are informed and comfortable with the consent process, they're more likely to comply with protocol, remain enrolled, and contribute to faster study deployment.
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Safeguarding Personal Data: Protecting PII
3/17/2025
Learn about a secure, patient-centric platform that enables individuals to participate in clinical trials and registries while maintaining lifelong access to their data.