“One of our large European pharmaceutical clients has been able to eliminate several global investigator meetings, allowing them to accelerate their trial,” says Tapio Schnaars, AxxiTRIALS® Product Manager. “They have also been able to easily on-board new sites and staff throughout the trial, reduce site monitoring visits and track the status to ensure compliance.”
AxxiTRIALS® automatically determines which users should receive what training based on geography, role and/or DoA code, and sends them simple email alerts with links to the training. Leveraging the simplicity and convenience of familiar web technology, users are able to simply view videos and other training material, provide confirmation of completion, take quizzes if needed and automatically receive certificates upon satisfactory completion of material.
AxxiTRIALS® gives users the freedom to take training when it is convenient for their schedule and location, work at their own pace, review complex topics and receive their certificates automatically. Automated reporting and audit trail ensure oversight and compliance.
AxxiTRIALS® speeds clinical trial operations from Feasibility to Close-out allowing studies to complete on time and on budget with the required quality of data. As a secure mobile portal, AxxiTRIALS® reduces trial start-up and operations management time throughout an entire project by automating tasks such as reports, alerts and archiving processes. AxxiTRIALS® reduces time spent at clinical research sites by PIs and study site coordinators by simplifying their technology experience with a single solution for all trial content and systems. With leaderboards, community tools, and live access to CRO staff, AxxiTRIALS® increases site engagement for internal staff. AxxiTRIALS® is the only portal to deliver real-time reporting of all KPIs, including a snapshot view of all leading and lagging indicators for full transparency into the status of sponsored trials.