One platform for every study in your pipeline
Trialflare gives contract research organisations a single, scalable platform to manage multiple concurrent studies without the enterprise price tag or months of onboarding. From eCRF to ePRO, eConsent to CTMS, everything your team and your sponsors need is in one place.
Run more studies with fewer tools, less overhead, and faster turnaround.
Get from protocol to first participant enrolled in days, not months.
Centralised oversight across your entire study portfolio.
Transparent costs that work for you and your sponsors.
"Trialflare is absolutely instrumental to our business. We're a fully remote CRO, but we operate in a highly regulated and compliant environment. Trialflare gives us a trusted research platform that is certified, compliant, and that the sponsors we work with genuinely trust."
Charlie Chadwick
CEO, Comet Clinical CRO
All-in-one platform
No more stitching together separate tools for EDC, consent, monitoring, and comms. Trialflare is modular, so you use what you need for each study.
Bespoke forms with validation, branching logic, and AI-supported building. Configure once, clone for repeat visits, and export clean datasets for your sponsors.
Digital consent with ID verification, video calling, and version control. WhatsApp, SMS, email, and push notifications to keep participants on track.
Multi-site coordination, visit scheduling, query management, and a built-in electronic trial master file. Everything audit-ready from day one.
Give your sponsors real-time visibility into their study with role-based dashboards. They see progress, data quality, and milestones without chasing you for updates.
GDPR, HIPAA, 21 CFR Part 11, ICH GCP, and Cyber Essentials Plus certified. UK/EU data centres, 2FA, role-based access, and full audit trails on every action.
Trialflare brings your entire study team together in one place.
Design eCRFs, manage queries, monitor data integrity, and export clean datasets for sponsors.
Remote monitoring, source data verification, site visit tracking, and real-time compliance dashboards.
Role-based dashboards with live enrolment, milestone tracking, and study performance at a glance.
Oversee participant safety, review adverse events, and approve protocol amendments from one platform.
One login for all study activities. eCRF entry, eConsent, document uploads, and task management in one place.
Statisticians, nurses, sub-investigators, ethics committees, and any other role your study requires. Trialflare adapts to your team structure.
Learn more about
See how Trialflare can help you deliver more studies, faster.
Schedule a demo
