eCOA Resources
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Smarter eCOA With Clinical ink
9/22/2022
Deploy a smarter, faster, simpler eCOA with Clinical ink, powered by deep outcomes science expertise across many therapeutic areas.
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Implementing Caregiver Assessments: Key Considerations
11/16/2023
When caregivers are involved in a clinical trial, remember to utilize these tactics to ensure that the completion of Observer Reported Outcomes is user-friendly and upholds data quality standards.
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Simplifying ePRO Data Collection
10/4/2024
The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.
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Improving The Patient Experience Through User-Focused Design
3/30/2023
Watch YPrime's Product Director of Decentralized Trial Technology and eCOA Product Innovation Karl McEvoy discuss the utilization of user-focused research on software design and implementation.
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Study Build And Scheduler Tools
3/27/2025
Empower your study participants with IQVIA eCOA’s tailored user experiences, flexible event triggers for clinicians, comprehensive training resources, and 24/7 support for seamless study management.
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C3 Summit Recap: Shaping The Future Of eCOA/ePRO Highlights
2/10/2022
Understand how the rapid shift to decentralized clinical trials required pharma companies and CROs to adapt data capture techniques quickly while remaining compliant with local regulations.
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Leveraging Tech And Clinician Review To Improve Risk Detection
10/19/2023
Learn why neuroscience therapy developers should start adopting strategies to improve data quality and assess responses using a combination of technology and expert clinician review.
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The Case For Cognitive Assessments In Phase 1 Clinical Trials
7/16/2024
Regulators prioritize patient-reported outcomes. Cognitive assessments in Phase 1 trials detect early drug-related cognitive effects, ensuring safety and efficacy. Signant’s CDR System® is a proven tool for this.
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Mitigating The Risks Of Long-Term Oncology eCOA Clinical Trials
6/23/2022
This article digs into the specific complexities of long oncology clinical trials and describes relevant solutions to manage the risks regarding patient compliance, clinical project teams, and clinical sites.
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Why eConsent Makes Such A Difference In Patient Adherence And Engagement
6/6/2022
Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.