ePRO/eCOA White Papers & Case Studies
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Technology And Scientific Expertise To Power Your Program
8/5/2024
Learn how our expertise in eCOA, RTSM, and eConsent solutions can accelerate your drug development program from early phases to regulatory approval.
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Capture And Transfer Up To 100% Of EHR-Based Data
7/23/2024
Flatiron Clinical Pipe™ eliminates manual data entry of structured and unstructured data—improving site workflows, lowering data monitoring costs, and enabling you to hit study milestones faster.
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Case Study: Using Technology To Reduce Operational Burden In Clinical Research
7/23/2024
The Beat AML® master trial is transforming treatment for people with acute myeloid leukemia (AML), already improving survival for patients enrolled in a Beat AML study vs. standard chemotherapy. Read this case study to learn how a proven EHR-to-EDC system has enabled the success of this impactful trial.
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Why Choose TrialKit For Your Clinical Trials?
7/18/2024
TrialKit supports everything from small biologics trials to large Phase 3 pharmaceutical trials and extensive registry studies, allowing you to capture and manage your clinical trial data as you see fit.
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Paper Vs ePRO: Clinical Data Collection Methods
7/16/2024
Patient-reported outcomes (PROs) assess patients' health without clinician interpretation. Traditional paper methods often result in missing data and quality issues, while electronic solutions enhance data accuracy and completeness.
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Adding RTSM To eCOA
7/16/2024
Using Signant SmartSignals® RTSM with our eCOA solution streamlines site workflows, eliminates data reconciliation, and simplifies operations for sponsors/CROs. It ensures eligibility before randomization, reducing protocol deviations.
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Get Your Tile Into One Home for Sites™
7/15/2024
When you "get your tile" into One Home, you're building up the library of systems available to sites for single sign-on and task management across their trials.
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Medable Platform Delivers >90% eCOA Adherence And Scalability
7/8/2024
Discover how eCOA use drove >90% adherence across an extensive weight management master protocol clinical trial with multiple sub-studies across 70+ research sites.
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Veeva eCOA Features Brief
6/24/2024
Ensure access and transparency throughout clinical studies while streamlining the design, management, and completion of electronic Clinical Outcome Assessments with Veeva eCOA.
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Powering Smarter Treatments And Healthier People
6/19/2024
Explore Medidata's commitment to transforming the life sciences sector, fostering patient-centric trials, and creating new opportunities for healthier populations globally.