Smart, Adaptive Randomization for Clinical Trials
Datacapt Randomization is a flexible, powerful module that simplifies even the most complex allocation strategies for randomization in clinical trials, fully embedded within the Datacapt EDC. With an intuitive interface and rapid setup, it gives your team the control, compliance, and speed they need, without the complexity.
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Datacapt turns randomization into a seamless part of your study workflow.
Randomization Made Simple
Supports block, stratified, dynamic, and minimization algorithms
Define allocation ratios, strata (e.g., age, site, disease type), and timing
Set up in minutes, with an intuitive interface
Directly integrated within the Datacapt EDC eCRF, no third-party system required
Fully Embedded in Your Study Workflow
Role-based masking ensures blind integrity for sites and sponsors
Instant, role-controlled emergency unblinding at site or sponsor level
Unified user experience for investigators and study teams
Real-time API access if needed for integration with external systems
Ready to Simplify Randomization?
Request a demo and see how Datacapt brings powerful, protocol-driven allocation strategies directly into your study environment—without complexity.
We support block randomization, stratified randomization, dynamic randomization (minimization), and more.
Yes. All allocation logic is fully validated under GCP and 21 CFR Part 11 guidelines. We support advanced methods like Pocock-Simon minimization to ensure balanced treatment arms, with full documentation, audit trails, and compliance-ready processes.
Yes. Our no-code randomization module allows changes (e.g., ratio, strata) with versioning and audit control—ideal for adaptive designs.
Yes, Randomization and supply modules are linked in real-time to prevent errors and streamline logistics.
The investigator randomizes the patient from the eCRF in a few clicks. The platform applies the imported list or the configured algorithm (blocks, stratification, minimization), manages blinding and records the allocation in the audit trail.
Yes. The module runs in the same platform as the eCRF and trial supply management, linked in real time. Your other systems receive the data through the REST API and webhooks.
An IWRS assigns patients to study arms. An RTSM adds trial supply management: stock per site, resupply, dispensing. Datacapt covers both, with randomization linked to trial supply management in the same platform.
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