ZELTA ECOA
Seamlessly collect clinical research data directly with Zelta eCOA
Empower clinical trials with intuitive eCOA technology that eliminates integration hurdles while enhancing patient experience and data quality.
Video
Fast tracking clinical trials with ePRO and self-service
Listen to Katrina Riggs, Chief Operating Officer for Fast-Track Drugs and Biologics, share how her team has leveraged Zelta's ePRO capabilities and self-service support to accelerate clinical trial timelines with dozens of patient-reported outcomes and put their clients' data management needs and drug development processes on the fast track.
Deliver the best experiences for clinical trial participants and site personnel
Built-in ePRO for seamless and efficient clinical trials
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Zelta’s eCOA solution is built directly into the platform. Enjoy single sign-on access for cohesive workflows, efficient data management, and improved data quality for clinical trial teams.
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Design and manage ePRO data collection forms, schedules, and rules directly within Zelta EDC, ensuring seamless setup for your team.
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Access Zelta ePRO anytime, anywhere with compatibility across browsers, iOS, and Android devices for ultimate flexibility.
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Customize workflows to the specific needs of your trial.
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Convenient, real-time patient-reported outcomes that deliver actionable insights and improve participant adherence.
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Zelta eCOA/ePRO captures data directly from clinical trial participants.
Enhance participant experience with real-time patient-reported outcomes
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Personalize engagement with participants and caregivers through real-time notifications and multilingual support.
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Optimize regulatory compliance while ensuring secure handling of patient data.
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Choose between bring your own device (BYOD) or issued-device compatibility for hybrid trials, depending on your needs.
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eCOA forms can be saved as drafts for the patient to complete when convenient for them.
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Replace traditional paper-based methods with an intuitive ePRO solution available on mobile devices to make questionnaires and data entry simple and stress-free for participants.
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Optimize data management and site experience with ePRO
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Optimize data management in clinical trials with ePRO solutions that enhance data quality, patient compliance, and safety.
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Improve data quality and streamline electronic clinical outcome assessment eCOA processes.
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Empower decision-making with real-time data on patient-reported outcomes and compliance feedback.
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Simplify data collection with a BYOD approach, issued devices, and flexibility for hybrid trials.
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Ensure seamless data entries and regulatory compliance with accurate timestamping and comprehensive audit trails.
Zelta eConsent: Quickly consent participants wherever they are
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Maximize site efficiency and remote management of participant consent for clinical trials.
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Manage eConsent directly from Zelta’s electronic data capture system, alongside the eCOA/ePRO module.
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Track amendments, consent status, and timelines in a dedicated dashboard.
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Increase participant convenience with single sign-on access to both eConsent and eCOA/ePRO.
eCOA and ePRO unleash the benefits of decentralized trials
Decentralized clinical trials (DCTs) offer several benefits for CROs and sponsor companies, including reduced need for site travel, lowered trial costs, and better patient-reported outcome data for analysis.
Enabling trial participants to report outcomes via ePRO or using eConsent can greatly improve the patient experience, boost recruitment for trial managers, and enable real-time data capture. The Zelta platform – including eCOA, ePRO, eConsent, and other modules – has been used to successfully build, run, and support over 250 hybrid trials or DCTs.
Ready to talk?
Speak with an Zelta specialist or see a solution demo.
