The studyOS platform helps lean teams catch study issues before they're issues in real-time, enabling comprehensive study oversight.
Supercharge your clinical trials with studyOS' comprehensive data solutions. Our platform revolutionizes trial management by automating the creation of custom reports and visually appealing graphs, eliminating the need for manual trackers and Excel sheets. With studyOS, you gain immediate access to crucial insights, streamlining decision-making processes and significantly boosting productivity.
Here's how we help streamline your operations:
Consolidate all clinical data from EDC, eCOA, ePRO, labs, and more into a single, user-friendly platform. Eliminate the need for multiple portals and passwords, ensuring streamlined data access and management.
Receive clear, actionable insights in plain English. studyOS quickly identifies potential deviations and issues, enabling faster root cause analysis.
Rapidly uncover critical relationships within clinical and operational data. Leverage these insights to accelerate strategic decision-making.
With our cutting-edge, risk-based monitoring solutions, your trials will achieve a higher level of safety and efficacy.
Rapidly uncover critical relationships within clinical and operational data. Leverage these insights to accelerate strategic decision-making.
Focus on the most critical data and processes, ensuring efficient and effective trial management.
Continuously update and adjust risk levels throughout the trial for optimal oversight and compliance.
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Harness AI-powered central monitoring to oversee trial activities, promptly identify irregularities, and maintain the highest standards of data quality and integrity.
Define and monitor KRIs and QTLs to maintain high standards and regulatory compliance throughout the trial lifecycle.
Automate inclusion/exclusion criteria checks and monitor retention rates to ensure proper enrollment and maximize participant engagement.
Unify information from multiple vendors into a comprehensive, single-source listing, dramatically reducing manual workload and boosting operational efficiency.
"As we approached the database lock for a phase III study, studyOS was instrumental in identifying datasets that required additional review.
They helped us avoid having to unlock the database and thus provided a instant ROI. I cannot recommend them enough."
Benefit from a platform designed by former FDA auditors, life science lawyers, Microsoft technologists, and clinical operations leaders, ensuring unparalleled compliance with patient safety and data integrity standards.
Create customized listings and dashboards that display the most important metrics for your clinical trial.
Leverage cutting-edge AI to enhance data quality, detect anomalies, and generate real-time, actionable insights for informed decision-making.
Our intelligent platform never sleeps, constantly analyzing data to detect and neutralize risks before they escalate. We're not just protecting data integrity and participant safety – we're setting new industry standards.
