Articles, App Notes, Case Studies, & White Papers
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Parkinson's Disease: Leveraging Wearable DHTs
10/22/2024
Wearable DHTs offer a solution to the challenges of measuring Parkinson's disease in clinical trials. Discover how these technologies can improve outcome measures and accelerate drug development.
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Training Program Reduces Placebo Effect By More Than 50% In ePRO Study
5/17/2023
Discover how an instruction program directly contributed to significantly lowering the placebo response rate in a phase III migraine CNS study.
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What Does EDC Look Like In 2024 And Beyond?
2/12/2024
Read along as industry experts from TrialKit offer insights into the anticipated developments and challenges surrounding electronic data capture.
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Medical Device Clinical Trials: Key Considerations For Sponsors And CROs
3/30/2026
Medical device trials must align risk class, regulations, and study design. Strong oversight, data, and proactive safety planning support reliable evidence and market approval.
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eConsent: The Missing Ingredient To More Engaging Clinical Trials
8/29/2022
Electronic consent promotes better trial experiences, but many sites and sponsors are wary of giving up paper-based processes. Consider their reasons for caution and how teams can prepare for the switch.
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Technology Fragmentation Is One Of The Biggest Hidden Risks In Clinical Trials
4/6/2026
Reclaim your research day by reducing manual data entry. Learn how connecting operational and financial workflows eases administrative burdens and supports site sustainability.
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FDA Guidance Has Implications For EDC And EHR eSource Capabilities
2/28/2023
Gain insight from an eSource study observing digitally received data as far back as 2007 to just before initial guidance was released by the U.S. FDA in 2013.
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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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To Counter Bias, Counterbalance
1/4/2022
It’s easy to overlook the effects a survey’s format can have on responses, but those effects are potent sources of bias. Modern EDC allows you to systematically vary both question and response option order. This practice, called counterbalancing, guards against unwanted order effects.
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5 Key Takeaways From The FDA's Real-World Evidence Guidance
8/19/2024
With our advanced technology and expertise, sponsors can confidently conduct RWE studies that are efficient and aligned with the FDA’s data-driven vision for healthcare.