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Accelerate clinical trial success with a platform that simplifies milestone tracking, document management, and regulatory compliance.
Managing clinical trials is complex, requiring meticulous coordination of milestones, documents, and compliance. ACE Clinical simplifies the entire trial lifecycle, helping organizations stay on schedule and in compliance.
Plan and monitor trial phases, setting milestones and dependencies to ensure timely progress.
Store and organize all trial-related documents within an electronic Trial Master File (eTMF).
Assign tasks, track progress, and ensure alignment across teams and stakeholders.
ACE Clinical ensures trials meet global regulatory requirements, reducing risks of noncompliance and delays.
Maintain a compliant, electronic Trial Master File that is always ready for regulatory inspection.
Connect trial activities to quality processes like CAPA and deviation management.
Prepare documentation for regulatory submissions, ensuring alignment with FDA, EMA, and ICH guidelines.
ACE Clinical helps organizations streamline trial operations, reduce costs, and accelerate timelines.
Monitor trial progress, document statuses, and milestone completions at a glance.
Simplify document handling within the eTMF for improved organization and accessibility.
Use insights to identify bottlenecks, improve processes, and ensure trial success.
Maximize the value of your clinical trial management with ACE®.
