Contact Sales Support Center
Ensure process integrity and regulatory compliance with a system that captures, investigates, and resolves deviations efficiently and transparently.
Deviations in life sciences processes can lead to compliance risks and operational inefficiencies if not addressed promptly. ACE’s Deviation Management ensures deviations are recorded, investigated, and resolved seamlessly.
Capture deviations consistently across processes, ensuring all necessary details are documented for traceability.
Tailor deviation types and workflows to align with your specific processes, such as manufacturing or clinical trial deviations.
Alert relevant stakeholders immediately when a deviation is logged, ensuring timely action.
ACE® equips teams with tools to investigate and resolve deviations effectively, minimizing disruption to operations.
Use built-in tools like 5-Why analysis to identify root causes.
Connect deviations to CAPA workflows and risk assessments to ensure corrective actions are effective.
Evaluate how deviations affect product quality, timelines, and compliance to prioritize resolution efforts.
ACE® ensures that deviation management processes meet the stringent requirements of global regulatory bodies.
Maintain comprehensive logs of all deviation activities, including investigations, actions taken, and final resolutions.
Track the status of deviations and related actions through intuitive dashboards.
Use analytics to identify trends in deviations and implement preventive measures.
A quality management system (QMS) is defined as “a collection of business processes focused on consistently meeting customer requirements and...
In regulated industries such as life sciences and healthcare, validating custom workflows for processes associated with Quality Management Systems, Training,...
In a regulated industry, good documentation practices are paramount to success. When your audit begins, often the first thing auditors...
Maximize the value of your deviation management with ACE®.
