eCRF.biz review
Configurable EDC with ePRO, randomization, validation, and clinical data controls.
Reviewed by iTechGuides Editors · Editorial team · Updated Oct 2026
eCRF.biz is BioStat’s electronic data capture and clinical data management platform for clinical trials, observational studies, and medical records. It is aimed at pharmaceutical and biotechnology research teams running single- or multicenter studies, particularly mid-market and enterprise organizations. Configurable electronic case report forms support study data collection, while query management, notifications, validation rules, audit trails, randomization, investigational drug management, and reporting cover core operational workflows. The platform supports FDA 21 CFR Part 11, GDPR, and HIPAA requirements and runs as a cloud service accessed through the web.
Pricing is quoted individually, and BioStat typically provides eCRF.biz through a study implementation service model. That approach can align the platform with a study’s forms, workflows, and data-management needs rather than relying on a fixed self-service package. The feature set is especially broad around regulated data capture: audit trails record questionnaire changes, timing, and authorship; field rules support validation; and queries can be managed with notifications. Dynamic study reports add an output layer for ongoing review.
eCRF.biz also connects ePRO data through synchronization with the EDC environment and supports laboratory integration and external data transfer. Randomization and investigational drug management extend its scope beyond form collection, making it suitable when study operations and treatment allocation need to sit in one system. Email and phone support are available. Teams seeking a configurable, service-led EDC with ePRO and trial-management capabilities should consider it; organizations requiring on-premises deployment, fixed published pricing, or a self-directed implementation model may prefer another option.
eCRF.biz pros and cons
- Where it wins
- Configurable eCRFs with field rules, validation, queries, and audit trails
- Supports ePRO synchronization, randomization, and investigational drug management
- Provides dynamic reports, laboratory integration, and external data transfer
- Where it doesn't
- Pricing is quoted individually through BioStat
- Cloud-based web deployment may not fit on-premises requirements
- ePRO mobile app preparation is available on request
eCRF.biz fact sheet, pricing and score →
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