Contact Sales Support Center
Address root causes and prevent recurrence with an integrated CAPA system that streamlines workflows, tracks progress, and supports regulatory compliance.
When quality issues arise, tackling them at the root is critical to maintaining compliance and safeguarding your operations. ACE CAPA Management simplifies every step, from identifying nonconformities to implementing long-term solutions. With ACE, you’re not just resolving problems—you’re preventing them from happening again.
Investigate issues thoroughly with built-in tools like 5-Why analysis to uncover root causes.
Connect CAPA records to related quality events, deviations, or audit findings for a holistic view of quality management.
Implement pre-configured, standardized workflows designed to meet GMP, FDA, and ISO requirements, or create fully customized workflows tailored to your needs.
Delays in implementing corrective and preventive actions can escalate risks and compliance concerns. ACE CAPA Management keeps your team on track by automating task assignments, setting clear deadlines, and ensuring actions are verified for effectiveness.
Assign corrective actions automatically to the right team members, complete with deadlines and real-time notifications.
Verify the effectiveness of implemented actions to ensure issues are fully resolved and won’t recur.
Alert stakeholders of upcoming deadlines or overdue tasks to prevent delays.
Regulatory compliance demands thorough documentation, transparency, and continuous improvement. ACE CAPA Management ensures your organization not only meets but exceeds these expectations, creating a culture of proactive quality management.
Maintain detailed, audit-ready records of every CAPA activity, from initiation to closure, to satisfy even the most rigorous inspectors.
Use advanced reporting and analytics to identify recurring patterns, assess CAPA effectiveness, and refine processes.
Foster a culture of improvement by integrating CAPA with risk assessments, change control, and training to address gaps and strengthen operations.
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 CAPA management with ACE®.
