Log the defect
Record part numbers, serials, lots, revisions, suppliers, production details, photos, and immediate containment.
Product Investigation Management Software
Pin down product issues from the first NCR to verified fix. CAPA Manager guides engineers through structured product investigations, evidence capture, root-cause analysis, corrective action, and reporting.
Record part numbers, serials, lots, revisions, suppliers, production details, photos, and immediate containment.
Run 8D, RCCA, 5 Whys, Ishikawa, and evidence-based analysis to identify cause and define actions.
Verify effectiveness, approve closure, and export professional investigation reports for customers, suppliers, and audits.
Replace ad-hoc spreadsheets with a guided product investigation process that keeps engineering, quality, production, and suppliers aligned in one product investigation management system.
Log NCRs, defects, lots, serials, dispositions, quarantine status, containment, photos, and documents.
Guide teams with 8D, RCCA, 5 Whys, Ishikawa, evidence review, and corrective action planning.
Generate clean product investigation, NCR, 8D, action, approval, and evidence packs for external communication.
Track repeat defects, scrap trends, overdue actions, supplier issues, and investigation cycle time.
CAPA Manager supports product investigation workflows for ISO 9001, AS9100, IATF 16949, ISO 13485, and supplier quality teams that need controlled records, traceable evidence, and verified corrective action.
Create a free CAPA Manager account and start managing product defects, NCRs, root-cause investigations, and corrective actions today.
Product Investigation Management Software digitises the process of identifying, investigating, and resolving product non-conformances. It connects NCR logging, root cause analysis, and corrective actions into one traceable workflow.
Manufacturing, quality, supplier quality, production, and engineering teams use Product Investigation Management Software to investigate product defects and verify corrective actions.
It guides users through structured 8D and RCCA steps, integrates root-cause tools, and generates reports for customers, suppliers, and auditors.
Yes. Suppliers can participate in controlled investigations while your quality team keeps oversight of evidence, actions, status, and closure.