Articles, App Notes, Case Studies, & White Papers
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What Happened At ASCO 2024
6/13/2024
Discover our associates' insights on the key developments from ASCO 2024 that are set to shape the future of cancer care and patient outcomes.
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How To Improve Patient Outcomes Using eSource Software In Clinical Trials
8/11/2025
As the demand for patient-centric clinical trials grows, eSource platforms will play an increasingly vital role in facilitating efficient, compliant, and innovative research methodologies.
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Inova Health System Uses Advarra eReg Workflows And Integrations To Improve Regulatory Efficiency
2/22/2021
Maintaining efficient, effective regulatory management processes can be a significant challenge. At Inova Health System, the research team improved regulatory efficiency by 20% without the need for extra regulatory staff by adopting Advarra’s eRegulatory Management System.
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Revolutionizing Pediatric Clinical Trials With ePRO And eConsent
10/16/2024
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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Evaluating EDC Systems In A Modern DM Landscape
6/24/2024
This guide provides five crucial recommendations to refine evaluation strategies and choose the right solution for today's complex clinical data environment, optimizing data collection practices.
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Breaking Down Barriers: Why Closed Technology Ecosystems Are Holding Back Clinical Research
5/24/2023
Explore the barriers created by closed technology ecosystems and the importance of open, interoperable solutions for advancing healthcare.
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How Medidata Link Is Supporting Moderna's Clinical Trial Real-World Data Linkage Initiatives
6/5/2024
Discover how Medidata Link empowers Moderna's clinical trial RWD linkage initiatives, enhancing insights into treatment outcomes while minimizing administrative burdens.
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Evaluating Wearable Data Platforms For Endpoint-Driven Studies
2/24/2026
Endpoint‑driven studies need platforms that unify wearable data with trial systems, support derived measures, and ensure traceability so continuous data becomes reliable clinical evidence.
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U.S. Renal Care Achieves 75% Site Adoption Of eConsent
5/1/2024
By dispelling prevalent misconceptions regarding participant age, cost, and complexity, see how this platform emerged as a versatile, rapid, and effective solution tailored to the unique needs of the elderly renal care population.
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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.