Cronos specializes in Risk-Based Data Monitoring (RBDM) of Clinician Reported Outcomes (ClinROs) in CNS trials to enhance signal detection. Using our proprietary AccuRate™ algorithms we provide realtime iterative analysis of 100% of scale data points to identify irregular and unusual data, inter- and intra-scale inconsistencies, unlikely deltas, and possible malfeasance. Flagged data are investiga
ted by our expert clinical team by direct interaction with the site raters in their local language, and review of recorded assessments; remediation and preventative actions are taken, with escalation where appropriate. Cronos mitigates risk to your trial by proactively identifying and managing sources of error. Cronos also offers an all-in-one software solution to the scheduling challenges of complex international clinical trials. The Cronos Integrated Research Platform (CIRP) simplifies criteria-based scheduling, incorporating patient’s availability, patient’s language, protocol visit windows, rater qualification/roles, rater availability, for both site-based and centralized raters. Using an independent platform can also prevent functional unblinding. CIRP was developed in-house specifically for pharmaceutical trials and features automatic localization in over 20 languages, full Outlook integration, automated time-zone changes, and role-based access levels.
