Clinical Trial Technology Case Studies and Fact Sheets
Explore how YPrime helps sponsors and CROs solve complex clinical trial challenges through configurable eCOA, IRT, and data-driven oversight. Our case studies and fact sheets provide real-world examples of faster study startup, improved data integrity, and confident execution across global trials. See how YPrime delivers speed, flexibility, and clinical trial certainty, backed by measurable outcomes.
eCOA and IRT Case Studies: YPrime in Action
eCOA Case Study: How YPrime Preserved Data Quality During a Phase 3 Oncology Protocol Amendment
How do you maintain data quality when clinical trial protocol amendments threaten study timelines? A…
YPrime eCOA for Clinical Trials: A Pediatric Migraine Study
For a global trial spanning over 200 sites with more than 800 participants, a pharmaceutical…
YPrime eCOA in Action: AI-Powered Clinical Trial Localization
When a leading pharmaceutical sponsor needed to add India to an ongoing trial after finalizing…
eCOA, eConsent and IRT Fact Sheets
YPrime Advanced eCOA Oversight
YPrime’s Advanced eCOA Oversight digitizes investigator review and sign-off to strengthen participant safety and compliance…
The YPrime Data Suite. eCOA Reporting Improves Decision Making.
YPrime’s Data Suite brings together advanced eCOA and IRT reporting with seamless data integration…
Audit-Ready eCOA Reporting to Improve Clinical Trial Decisions.
YPrime’s eCOA and IRT reporting delivers live insights and unmatched speed to help trial teams…
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