GxP-compliant from protocol to close-out
Trialflare is built for regulated clinical trials. Manage the full trial lifecycle with compliant eCRF, ePRO, eConsent, CTMS, and eTMF in a single platform. Coordinate across multiple sites, maintain audit-ready data, and deliver trials remotely or on-site.
Deliver compliant, audit-ready trials at scale with a single integrated platform.
Built to meet the highest regulatory standards.
Manage complex multi-site trials from one place.
One platform for the entire trial lifecycle.
GxP compliant
Every feature in Trialflare is designed for compliance. From protocol-driven data capture to electronic signatures, your trial data is audit-ready from day one.
Build case report forms that mirror your protocol. Branching logic, edit checks, and real-time validation ensure clean data capture at every visit.
Deliver informed consent documents electronically with compliant e-signatures, version control, and full audit trails. Support for remote and in-person consent.
Organise essential documents in a structured electronic trial master file. Track completeness, manage versions, and stay inspection-ready throughout the trial.
System-generated and manual queries with full tracking, escalation, and resolution workflows. Reduce data cleaning time and close queries faster.
GDPR, HIPAA, 21 CFR Part 11, ICH GCP, and Cyber Essentials Plus certified. UK/EU data centres with full audit trails.
Learn more about
See how Trialflare brings compliance, coordination, and data quality together in one platform.
Schedule a demo
