Patient Data Reporting Applications & Studies
-
DTx Company Leverages Real-World Evidence Platform In Registry Study
8/19/2024
Discover how Castor’s eClinical system enabled a groundbreaking study in behavioral disorder treatment to collect Real-World Evidence (RWE) to support product research and claims.
-
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.
-
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.
-
Cancer Research UK's Path To Rave EDC And The Medidata Platform
6/17/2024
Discover how Cancer Research UK, the world's largest cancer charity, upgraded to Medidata's Rave EDC platform, streamlining clinical trials and enhancing productivity while ensuring minimal disruption.
-
Our Unified Platform Serves As eSource For COVID Treatment Trial
6/17/2024
Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.
-
eCOA: Unified Approach Streamlines Processes, Speeds Start Up And Improves Data Quality
5/8/2024
Discover how a leading biopharmaceutical company revolutionized its clinical development with an eCOA solution that optimized its processes, cut build times, and enhanced data quality.
-
Vaccine Trial Sees >90% eCOA Adherence
5/1/2024
Discover how we addressed vaccine trial challenges and drove remarkable success, achieving over 90% adherence to eCOA, ensuring active engagement from the trial participants, and yielding consistent, reliable trial data.
-
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.
-
The Business Case For EHR eSource In Clinical Trials
4/12/2024
Examine how manual data collection challenges prompted the adoption of an eSource solution that streamlined data entry, saving time and costs, reducing errors, and accelerating a multicenter phase 2 trial.
-
Mobile App And Wearable Integration Collects Longitudinal Data
2/12/2024
Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.