Clear Nonconformity Statement
Record the requirement, nonconformity, objective evidence, source, process, site, severity, owner, and due date.
QT360 CAPA and RCCA Software
Corrective Action and Root Cause Analysis Software
Control nonconformity response from objective evidence and containment through root cause, corrective action, approval, and effectiveness verification.
The Problem QT360 Solves
Keep the Entire Process Connected
A corrective action is not complete just because an action item was closed. Quality teams need a clear line from the requirement and evidence to the verified cause, completed action, approval, and effectiveness result.
ISO 9001AS9100AS9110Browser-BasedAudit Evidence
What Quality Teams Gain
- Separate correction from corrective action
- Prevent vague root-cause statements
- Assign clear owners and due dates
- Keep approval evidence with the record
- Track effectiveness instead of closing too early
What This QT360 Module Controls
Structured records, ownership, status, due dates, and evidence for the complete workflow.
Containment and Correction
Separate immediate containment and correction from the longer-term action needed to prevent recurrence.
Five-Why Analysis
Document why-one through why-five and summarize the verified root cause.
Corrective-Action Plan
Assign action ownership, planned actions, related process, related risk, and completion responsibility.
Approval Control
Track approval status, approver, approval date, and related comments.
Effectiveness Review
Define the effectiveness method, record results, and retain evidence showing whether recurrence was prevented.
Built for Objective Evidence
QT360 is designed to make records easier to retrieve, review, and present during internal, customer, regulatory, and certification audits. The system keeps the process information together rather than spreading it across email, spreadsheets, and shared folders.
Standards Alignment
Support the Process—Do Not Treat Software as Certification
QT360 supports records and workflows commonly used to meet ISO 9001, AS9100, and AS9110 requirements. The organization remains responsible for determining applicable requirements, maintaining effective processes, evaluating results, and providing valid objective evidence.
Practical advantage: Aero Assured Solutions can support both the software setup and the quality-system process behind it.
Related QT360 Modules
Connect this process to the rest of the quality management system.
Internal Audit SoftwarePlan audits, capture evidence, issue findings, and track follow-up.Document Control SoftwareManage controlled documents, revisions, approvals, and review dates.Training Management SoftwareTrack job tasks, qualifications, due dates, and competency evidence.Risk Management SoftwareMaintain risks, opportunities, actions, owners, and effectiveness reviews.Management Review SoftwareOrganize required inputs, leadership decisions, outputs, and action items.Supplier Management SoftwareControl supplier approval, scope, risk, monitoring, and re-evaluation records.
Frequently Asked Questions
Clear answers about QT360 and the quality-system process covered on this page.
Does QT360 support five-why root cause analysis?
Yes. The corrective-action record includes why-one through why-five fields and a root-cause summary.
Can QT360 manage audit findings and customer issues?
Corrective actions can be opened from audit findings, nonconformities, complaints, or other QMS sources, with the applicable source and evidence recorded.
What is an effectiveness check?
An effectiveness check confirms whether the corrective action actually prevented recurrence or controlled the identified cause. QT360 records the planned method and the result.
Does QT360 guarantee a corrective action will be accepted by an auditor?
No. Acceptance depends on the facts, evidence, requirement, root-cause quality, implementation, and auditor or customer judgment. QT360 provides structure and traceability.
See QT360 With Your Own Quality-System Workflow
Schedule a guided demonstration focused on your standard, processes, records, due dates, and audit evidence.