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Active trials supported worldwide
Active trials supported worldwide
TAET centralizes adverse event intake, review, and reporting so sponsors, CROs, and investigators can respond without delay. From monitoring decentralized trials to managing complex oncology protocols, TAET keeps study teams aligned and compliant.
TAET is engineered for regulated environments, ensuring participant safety, transparent collaboration, and reliable data for regulators.
Capture adverse events through investigator portals, EHR integrations, and mobile reporting with automated routing to the right reviewers.
Generate MedDRA coding, FDA/Health Canada submissions, and sponsor notifications with configurable templates and audit trails.
Visualize safety trends, cohort-level risk, and study performance with dashboards that inform Data Safety Monitoring Boards.
Keep sponsors, CROs, and investigators aligned
Bridge safety, operational, and patient-reported data by connecting TAET with CareRelay care coordination and the national XGCHealth HIS platform. Unified governance keeps every handoff documented while preserving strict privacy controls.
TAET streamlines collaboration from site activation through study close-out, with configurable checkpoints that match your operating procedures.
Centralize training logs, delegation forms, and activation checklists so investigators can submit safety events on day one.
Automate alerts for protocol deviations and serious adverse events with configurable routing rules and on-call escalation.
Coordinate medical monitors, DSMBs, and regulatory submissions with audit trails, electronic signatures, and templated narratives.
Feed insights back into risk assessments, SOP updates, and future study designs with dashboards and exportable data sets.
TAET accelerates response times while maintaining uncompromising oversight for sponsors and regulators.
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Configurable queues and alerts reduce review cycles from days to hours, keeping participants protected.
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Automated document generation and electronic signatures simplify submissions to ethics boards and regulators.
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Role-based dashboards keep sponsors, DSMBs, and regulators aligned with up-to-date evidence.
Partner with XGC to onboard your studies quickly, integrate with electronic data capture systems, and align TAET with your regulatory strategy.