Decentralized Trial Technology Resources
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Evidence Generation Evolved
6/13/2024
Explore how innovative strategies are cutting clinical trial times in half and accelerating the delivery of life-saving treatments.
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Data-Driven Adaptive Trials Enhance Safety, Progress, And Economics
7/21/2023
By offering guidance on optimizing ROI from extensive data collections and various endpoints in clinical studies, learn how IRT technology can enhance the data-driven approach for sponsors.
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eCOA/ePRO: Why Patients Deserve Even More Progress
5/11/2022
The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.
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Beyond Integration: Flexible Orchestration Of IRT And eCOA Solutions
4/25/2023
Consider how integrated response technologies and electronic clinical outcomes assessments can improve configurability, study start-up, and flexible mid-study changes.
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Beyond The Pandemic: Why eCOAs Are Here To Stay
4/29/2022
The permanent adoption of eCOA is a natural step in the industry-wide effort to create a more patient-centric clinical trial experience. Learn more in the available blog.
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4 Ways Home Visits Support Successful Rare Disease Clinical Trials
4/25/2023
Researchers, patients, pharma, and regulators face several obstacles when designing and conducting rare disease trials. Here, we delve into the importance of home visits in rare disease clinical trials.
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Managing Drug And Data Requirements In Decentralized Clinical Trials
9/15/2025
Running a global decentralized clinical trial requires a deep understanding of the differences in FDA and EMA requirements for investigational products and patient data.
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Recommendations For Optimizing Televisits
6/6/2022
Discover the pros and cons of telehealth visits and what can be done to continuously improve them.
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Driving Customer Profitability With Enterprise Platform, Pricing
2/29/2024
Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.
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A Better Approach To eConsent: Flexibility With Enabled Technology
1/11/2023
Electronic consent, or eConsent, digitalizes the trial participant consent process through increasingly simplified, interactive, educational models designed to improve comprehension and boost engagement.