Discover how aChiral Chronos enables you to eliminate spreadsheets and manual processes, centralizing visit scheduling, patient reminders and audit traceability in a single integrated ecosystem, validated and compliant with GCP and ICH E6 (R2) regulations.
aChiral Chronos is the next-generation platform that revolutionizes patient follow-up in clinical trials, seamlessly integrating into the aChiral ecosystem. It provides a comprehensive environment for the control, supervision and traceability of every phase of the protocol, ensuring maximum regulatory safety and full compliance.
Define visit protocols once and let aChiral Chronos handle the rest. Configure flexible visit windows for each patient and site, with automatic protocol deviation detection and integrated multi-site calendar.
Multi-Level Reminder Engine
Automate patient communication through a three-level reminder system, at 15, 7 days and on the day of the visit itself. Email distribution personalized by site, with complete delivery status traceability and configurable distribution lists per study.
Deviation Detection and Multi-Site Management
aChiral Chronos automatically detects visit window violations and generates compliance reports with cause notes. Simultaneously manage unlimited sites, assign routes by geographic area and maintain centralized control over every study site with dedicated dashboards for CRAs and Project Managers.
Complete Audit Trail and Regulatory Compliance
Every action is recorded with full attribution, timestamp and rationale. aChiral Chronos ensures complete traceability from patient enrollment to study completion, with 4 independent confirmation pathways, native integration with aChiral ecosystem platforms, and possible integration with EDC and CTMS systems.
Who uses aChiral Chronos?
Designed for teams managing patient follow-up in multi-site clinical trials.
CRO
Manage follow-up across multiple studies and distributed sites with centralized visibility and automated reporting for each sponsor.
Sponsor
Monitor protocol compliance and adherence in real time across all sites, with executive dashboards and automated alerts.
Academic Sites
Simplify the operational management of follow-up for research institutions with standardized processes and minimal training required.
Data Manager
Access detailed reports, regulatory exports and quality dashboards for advanced data supervision across every study.
Maximize the Management of Your Studies' Follow-Up
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