Triall
Triall is dedicated to advancing clinical research through innovative, patient-centric technological solutions. They offer a comprehensive suite of eClinical software and services, including electronic data capture, clinical trial management, electronic trial master file, eSource, eConsent, ePRO, wearable integration, medical coding, clinical adjudication, blockchain proof, and more. Their platform supports remote data collection, decentralised and hybrid trials, and promotes data integrity, compliance, and operational efficiency. Triall collaborates with leading institutions like Mayo Clinic and partners in the digital health ecosystem to foster innovation and improve clinical trial processes.
Industries
Nr. of Employees
small (1-50)
Products
Electronic Data Capture (EDC) system
Interoperable EDC with drag-and-drop form builder, conditional logic, version control, query handling, SSO and integrations to other study modules for rapid deployment and data collection.
Direct data entry (eSource)
Mobile and web eSource for sites to enter source data directly, supporting multimedia, eSignatures and real-time synchronisation with the study database.
ePRO / eCOA
Patient-facing mobile surveys with reminders, safety notifications and wearable integration for remote PRO collection and oversight.
Electronic informed consent (eConsent)
Configurable consent forms with multimedia and conditional workflows that can be accessed and tracked remotely throughout the study lifecycle.
Clinical Trial Management System (CTMS)
Toolset to plan, manage and monitor study activities with reporting, site document access, workflow management and role-based permissions.
Electronic Trial Master File (eTMF)
Centralised environment for filing, managing and tracking trial documents with audit trails, mobile access and DIA TMF Reference Model structure.
Electronic Data Capture (EDC) system
Interoperable EDC with drag-and-drop form builder, conditional logic, version control, query handling, SSO and integrations to other study modules for rapid deployment and data collection.
Direct data entry (eSource)
Mobile and web eSource for sites to enter source data directly, supporting multimedia, eSignatures and real-time synchronisation with the study database.
ePRO / eCOA
Patient-facing mobile surveys with reminders, safety notifications and wearable integration for remote PRO collection and oversight.
Electronic informed consent (eConsent)
Configurable consent forms with multimedia and conditional workflows that can be accessed and tracked remotely throughout the study lifecycle.
Clinical Trial Management System (CTMS)
Toolset to plan, manage and monitor study activities with reporting, site document access, workflow management and role-based permissions.
Electronic Trial Master File (eTMF)
Centralised environment for filing, managing and tracking trial documents with audit trails, mobile access and DIA TMF Reference Model structure.
Services
Patient recruitment
Support for planning and executing participant recruitment strategies for clinical studies.
Data management
Operational data management services covering study data flow, cleaning, coding and integration with eClinical systems.
Regulatory affairs
Advisory and operational support for regulatory submissions and compliance activities.
Quality management
Quality assurance and quality management services to maintain inspection readiness and compliance.
Clinical trial management
End-to-end operational management of clinical studies, including oversight, site coordination and monitoring.
Clinical trial design
Study design services including protocol development and feasibility assessment, with support for data-informed protocol development.
Patient recruitment
Support for planning and executing participant recruitment strategies for clinical studies.
Data management
Operational data management services covering study data flow, cleaning, coding and integration with eClinical systems.
Regulatory affairs
Advisory and operational support for regulatory submissions and compliance activities.
Quality management
Quality assurance and quality management services to maintain inspection readiness and compliance.
Clinical trial management
End-to-end operational management of clinical studies, including oversight, site coordination and monitoring.
Clinical trial design
Study design services including protocol development and feasibility assessment, with support for data-informed protocol development.
Expertise Areas
- eClinical systems integration
- Clinical trial management and operations
- Decentralised and hybrid clinical trial execution
- Clinical data integrity and auditability
Key Technologies
- Electronic Data Capture (EDC)
- Direct data entry (eSource)
- ePRO / eCOA mobile data collection
- Electronic informed consent (eConsent)