Assign ownership and bring the right people into the investigation.
8D investigation software
8D CAPA Software for Root-Cause Investigation & Corrective Action
Guide teams through containment, root-cause analysis, corrective action, verification, and closure without losing evidence, ownership, or momentum.
- ContainmentCapture immediate action, ownership, risk, and evidence.
- Root causeUse 5 Whys, Ishikawa, RCCA, and structured 8D steps.
- ReportsExport audit-ready 8D reports with approvals and history.
Describe the issue clearly with evidence, scope, and impact.
Control immediate risk while the investigation is underway.
Use structured tools to find cause, not just symptoms.
Plan, verify, prevent recurrence, and close with a complete record.
8D software for RCCA investigation management
CAPA Manager 8D software offers investigation control in the cloud. Assign new issues to both internal employees and external suppliers instantly. It guides users through the 8D workflow: request, containment, root cause analysis, and solution deployment. Full 8D reports can be generated with a single click.
Trusted by thousands of users worldwide, this 8D software is one of the most effective solutions on the market today.
Investigation and corrective action reporting
CAPA Manager 8D Root-Cause Investigation & Corrective Action (RCCA) software automates assignment, notification, investigation, reporting, and approval of corrective actions from initiation to closure.
RCCA (Root Cause Corrective Action) software in the cloud
Connect teams, remote sites, and suppliers through a single corrective action system so geographically separated groups can interact with active investigations.
Standards-ready investigation management
Support auditable 8D and RCCA records for AS9100, IATF 16949, ISO 13485, GMP, and ISO 9001 environments with controlled root-cause evidence, corrective actions, workflow history, approvals, and effectiveness checks.
Maximum team engagement
CAPA Manager simplifies issue collaboration with internal and external teams, requires minimal training, and is ready to deploy quickly.
RCCA investigation management in the cloud
CAPA Manager 8D software helps teams manage internal quality events, supplier issues, customer complaints, audit findings, and corrective actions using one controlled workflow.
Instant visibility of status, ownership, and actions
Replace paper, spreadsheets, and disconnected email trails with live investigation status, reminders, dashboards, and clear responsibility for each action.
Designed for engagement
CAPA Manager is built for users who need to participate quickly. Guided screens, task ownership, and simple reporting keep investigations moving.
Produce complete 8D reports
Every decision, action, file, approval, and verification step is captured as the investigation progresses. When the team needs a report, the record is already there.
- Full 8D workflow access
- Collaboration with internal teams and external suppliers
- Compliance support for controlled investigation records
- Real-time dashboard and PDF reporting
Start using CAPA Manager today
Create your free account, open a guided 8D investigation, and see how CAPA Manager keeps ownership, evidence, actions, approvals, and reporting together.
Root cause analysis software for RCCA and 8D investigations
CAPA Manager works as root cause analysis software for manufacturing, supplier quality, aerospace, automotive, medical device, and regulated quality teams. Use structured RCCA software workflows to capture containment, analyze causes, assign corrective actions, verify effectiveness, and produce complete 8D reports.
8D software for AS9100, IATF 16949, ISO 13485, GMP, and ISO 9001 teams
CAPA Manager helps quality teams run 8D investigations and RCCA workflows with the records auditors expect to see: containment, root-cause analysis, corrective action plans, owners, due dates, evidence, approvals, verification, and closure history.
AS9100 8D software
Support aerospace corrective action and supplier quality investigations with traceable NCR, RCCA, containment, and effectiveness records.
IATF 16949 8D software
Manage automotive supplier 8D reports, manufacturing nonconformities, root cause analysis, action ownership, and verified closure.
ISO 13485 CAPA investigations
Help medical device teams keep complaint, nonconformity, supplier, and CAPA investigations controlled and audit-ready.
GMP CAPA and deviation support
Give GMP quality teams structured deviation, CAPA, RCA, approval, electronic record, and effectiveness-check workflows.
ISO 9001 corrective action
Document nonconformity response, cause analysis, corrective action, and effectiveness review in one searchable record.
Supplier RCCA workflow
Invite suppliers into controlled 8D actions while keeping ownership, evidence, status, and closure visible to your quality team.
Built for structured problem solving
Give teams a practical route from first report to verified corrective action.
Containment control
Record temporary actions and immediate protections while permanent corrective action is investigated.
Root-cause tools
Use 5 Whys, Ishikawa, and risk-based thinking to understand recurrence and prevention.
Supplier collaboration
Invite external users into controlled actions without losing traceability or oversight.
Approval gates
Use review and closure sign-offs to keep investigations compliant and auditable.
Launch your first 8D report within minutes
Start with a free CAPA Manager account and see how quickly your team can move from issue capture to structured corrective action.
CAPA Manager 8D software trusted by quality teams
CAPA Manager is rated 5.0 out of 5 from 8 customer reviews on Repuso review feed.