Discover the power of Zelta EDC
Unleash the power of Zelta, the cloud-based electronic data capture solution designed to give you control at every stage and confidence in every outcome of your clinical trials.
Video
Building studies with complex dynamics in 1 week
Rob Sandefur, former Principal Clinical Database Programmer for Lexitas Pharma Services, shares how Zelta has empowered his team to build clinical trial studies encompassing complex dynamics in as quickly as one to two weeks.
Features
Built for your unique clinical study challenges
Built with all users in mind, Zelta modules are fully integrated and share one code base across a unified platform – streamlining clinical trial processes and maximizing patient, caregiver, and provider engagement to accelerate outcomes and bring your treatments to market faster.
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eConsent
Deliver quick and easy remote consent with no integration needed.
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eCOA/ePRO
Advanced built-in ePRO, with significant dynamics and flexibility to engage directly with participants and caregivers via in-app assessments and real-time analysis.
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Medical coding with AI
Dramatically streamline the coding process, enhance accuracy, and ensure compliance with regulatory standards.
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Local Labs
Ensure data accuracy and integrity by standardizing lab data across sites when frequent sampling and fast results turnaround are essential.
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RTSM
Streamline processes so you can manage with ease.
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Globalization
Make site data collection and ePROs accessible, accurate, and compliant across multiple languages and regions.
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eLearning
Manage study training electronically to ensure regulatory compliance.
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CTMS (Powered by BSI)
Deliver comprehensive, easy-to-use functionality for all aspects of your clinical trials.
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eTMF (Powered by BSI)
Everything you need to capture and maintain regulatory binders and documents.
Deliver quick and easy remote consent with no integration needed.
Advanced built-in ePRO, with significant dynamics and flexibility to engage directly with participants and caregivers via in-app assessments and real-time analysis.
Dramatically streamline the coding process, enhance accuracy, and ensure compliance with regulatory standards.
Ensure data accuracy and integrity by standardizing lab data across sites when frequent sampling and fast results turnaround are essential.
Streamline processes so you can manage with ease.
Make site data collection and ePROs accessible, accurate, and compliant across multiple languages and regions.
Manage study training electronically to ensure regulatory compliance.
Deliver comprehensive, easy-to-use functionality for all aspects of your clinical trials.
Everything you need to capture and maintain regulatory binders and documents.
