Capture the issue
Record nonconformities, complaints, audit findings, observations, and improvement opportunities with consistent, searchable data.
CAPA Manager software
Manage corrective actions, root-cause investigations, approvals, evidence, and closure in one clear cloud-based workflow.
Record nonconformities, complaints, audit findings, observations, and improvement opportunities with consistent, searchable data.
Assign owners, gather evidence, identify root cause, plan actions, and keep every decision connected to the investigation.
Use approvals, verification, digital signatures, and complete history to prove that actions were completed and effective.
CAPA Manager helps teams control corrective and preventive action from first report through investigation, action planning, effectiveness review, and final closure.
Improving quality and maintaining compliance requires an effective Corrective and Preventive Action management system (CAPA). The CAPA process allows teams to capture and record problems like nonconformities, deviations, observations, and improvement opportunities, then assign responsibility for identifying the root cause and implementing corrective actions.
The CAPA process can improve operating processes from manufacturing to marketing. CAPA Manager enables organizations to manage quality performance and improvement across the entire operation quickly and effectively, enhancing quality, safety, and overall process compliance.
Automate the assignment, notification, investigation, reporting, and approval of corrective actions. CAPA software error-proofs the control of the corrective action process from initiation to investigation and closure.
CAPA Manager helps your organization take control of corrective action and improvement processes with a controlled, audit-ready, easy-to-use software solution designed to boost team engagement and reduce overhead.
Get started in minutes. CAPA Manager is cloud-based CAPA software with no installation delay, clean screens, and built-in workflows for quick adoption.
Track quality incidents from initial reporting through investigation and corrective action deployment, with a real-time view of tasks in progress.
Use one system for workflow control, notifications, investigation tools, approvals, evidence, reporting, and secure records.
Support CAPA, 8D, RCCA, A3, DMAIC, PDCA, audits, HSE events, and improvement projects.
Keep action owners, reviewers, and approvers moving with timely reminders and escalations.
Use 5 Whys, Ishikawa analysis, risk matrices, prioritization, and labels to understand recurring issues.
Protect approvals and closure with secure, traceable sign-off steps for validated records.
Attach files, documents, images, and supporting evidence directly to investigations and actions.
Track progress, overdue work, improvement trends, and data needed for audits or management review.
Effective corrective action depends on understanding cause, risk, and recurrence. CAPA Manager gives teams practical RCCA tools so investigations move beyond symptoms and into sustainable prevention.
CAPA Manager supports corrective action software, corrective action management software, CAPA management software, root cause analysis software, NCR software, supplier corrective action software, audit corrective action software, and cloud CAPA software search intent from one connected product page.
Manage nonconformities, investigations, actions, owners, due dates, approvals, and effectiveness checks. See corrective action software.
Use 8D, 5 Whys, Ishikawa, containment, corrective action, and verification to prevent recurrence. See 8D and RCCA software.
Convert audit findings and non-conformities into assigned corrective actions with evidence and closure tracking. See audit action software.
Coordinate supplier 8D reports, SCAR workflows, evidence, approvals, and response tracking. See supplier corrective action software.
CAPA Manager supports auditable corrective action workflows for quality teams working under ISO 9001, AS9100, IATF 16949, ISO 13485, and GMP expectations. It does not certify your organization by itself; it helps you keep the CAPA records, evidence, approvals, and effectiveness checks needed to demonstrate control.
Record nonconformities, investigate root cause, assign corrective actions, verify effectiveness, and keep documented information ready for audit.
Support aerospace NCR, RCCA, supplier corrective action, containment, approval, and recurrence-prevention records.
Manage automotive 8D reports, supplier issues, manufacturing NCRs, root-cause evidence, and verified corrective action closure.
Help medical device teams connect nonconformities, complaints, supplier issues, CAPA records, approvals, and traceable quality history.
Support deviation, CAPA, RCA, electronic record, digital signature, approval, and effectiveness-check workflows for GMP quality teams.
Use structured 8D and RCCA workflows across all standards so teams capture containment, cause, correction, prevention, and closure.
Get access to CAPA Manager and see how quickly your team can begin managing corrective actions in a structured workflow.
No sales calls. No Credit Card Required. Just instant access to your CAPA Manager account.
CAPA Manager is rated 5.0 out of 5 from 8 customer reviews on Repuso review feed.