Triall’s eClinical solutions are designed to support any therapeutic area, study design, and study phase. The platform offers advanced web-based, mobile, and wearable integration capabilities to support remote data collection and study management from anywhere, anytime.
Triall EDC allows you to rapidly build, deploy, and manage study forms from any device and any location.
Triall CTMS allows you to harmonise clinical trial management and oversight across all key study activities.
Triall eTMF provides a single secure environment for managing trial-related documents and ensuring inspection readiness throughout the clinical trial lifecycle.
Empower your sites with a flexible eSource solution for direct data entry.
Triall eConsent allows you to remotely onboard and engage patients for your clinical studies.
Triall ePRO offers a convenient and easy-to-use solution for carrying out surveys.
Tap into the power of wearables and access a wide range of health and fitness data, such as physical activity, heart rate, sleep patterns, and much more.
Triall Payments Manager helps promote site engagement by ensuring timely reimbursement based on tasks completion.
Seamlessly conduct and oversee all your medical coding activities from any device and any location.
Enjoy the benefits of a clinical endpoint adjudication solution that is fully integrated into the eClinical platform.
Triall Reporting & Analytics enables timely intervention and a risk-based approach to clinical trial management and oversight.
Triall RTSM allows you to randomise patients and manage trial supply using a combination of integrated tools.
Triall Virtual Visit offers a plug-and-play solution for remote engagement of study participants.
Leverage our Machine Learning API for true EHR-EDC interoperability.
Generate an immutable and system-independent audit trail of your clinical trial data and documents.
Our product specialist is available to answer all of your questions. Reach out to us to talk or to schedule a live product demo today.
Incredibly easy to set up, use, and reuse across studies. Design and deploy regulatory compliant studies in days.
All modules work together seamlessly. A unified platform to support your trials end to end.
Select modules based on your specific needs. Offered under flexible pay-per-study subscription plans.
All eClinical solutions to support you from study startup through close-out and beyond.
Truly supportive of hybrid and decentralised clinical trials. Work from anywhere, anytime.
Compliance with 21 CFR Part 11, GDPR, HIPAA, EU GMP Annex 11, ICH Q9, ISO 9002: 2015, ISO/IEC 27001:2013, SOC Type 2, and HITRUST.