Record the supplier issue
Document the nonconformity, affected product or process, supplier contact, evidence, and required response.
Supplier quality, 8D and SCAR
CAPA Manager helps supplier quality teams investigate nonconformities, manage Supplier Corrective Action Requests (SCARs), coordinate 8D investigations, and track corrective actions through to closure.
Start free with 2 users. No credit card required. No trial expiration.
SCAR and 8D explained
A Supplier Corrective Action Request is a formal request for a supplier to investigate a quality problem and implement corrective action. The 8D methodology provides a structured approach for defining the problem, recording containment, investigating root causes, and documenting corrective actions.
Keep each stage visible while your team coordinates the supplier response and maintains the internal record.
Document the nonconformity, affected product or process, supplier contact, evidence, and required response.
Record immediate containment, risk controls, and the information needed to protect customers and operations.
Use structured 8D, 5 Whys, and Fishbone tools to examine causes and supporting evidence.
Give actions clear owners and target dates, with responsibilities visible to the internal coordinator.
Track action status, due dates, reminders, comments, and evidence as the response develops.
Record implementation evidence, effectiveness-review findings, approvals, and the controlled closure decision.
Spreadsheets and email can be useful for managing individual supplier issues, but coordinating multiple investigations can become difficult as responsibilities, deadlines, and supporting evidence accumulate.
CAPA Manager keeps investigations, corrective actions, and follow-up activities connected, helping supplier quality teams maintain visibility and control.
CAPA Manager supports Supplier Quality Assurance (SQA) teams, purchasing, engineering, production, and quality management with a shared view of supplier issues, actions, decisions, and due dates.
Guide teams through problem definition, containment, root-cause analysis, corrective action, follow-up, and closure.
Record the internal coordinator and supplier contact, set response targets, and make overdue internal work visible.
Use 5 Whys, Fishbone, and structured 8D steps to document potential causes and the evidence behind decisions.
Assign actions, monitor completion, record review decisions, and maintain a traceable approval and closure history.
Keep supplier issues connected with related complaints, audits, incoming inspection findings, and corrective action records.
Use CAPA Explorer, dashboards, and filters to find records, monitor open work, and review recurring issue categories.
Evidence and reporting
Bring the supplier issue, investigation, action history, review findings, and closure decision together so teams can understand what happened and what remains open.
CAPA Manager provides general CAPA dashboards, searchable records, and CAPA Explorer filtering. These tools help teams review supplier-related records alongside other corrective action activity.
Supplier issues vary by industry. These examples show how a structured SCAR or 8D record can support investigation and follow-up without promising compliance on its own.
Record a supplied-component nonconformity, containment activity, investigation evidence, corrective actions, and follow-up decisions.
CAPA software for aerospaceCoordinate an 8D investigation for an incoming defect, with clear problem definition, action ownership, dates, and evidence.
Automotive corrective action softwareMaintain a structured response when purchased materials, services, tooling, or processes contribute to a quality issue.
Manufacturing quality softwareManage supplier investigations, corrective actions, root cause analysis, and follow-up in one structured system.
Start free with 2 users. No credit card required. No trial expiration.
It helps quality teams record supplier issues, coordinate investigation and containment, assign corrective actions, track dates, and maintain a traceable history through review and closure.
A SCAR is a formal request for a supplier to investigate and respond to a quality issue. An 8D is a structured investigation method that can be used to organize the response.
Yes. Internal quality teams can use CAPA Manager to maintain structured SCAR and supplier 8D records with owners, dates, actions, reminders, approvals, and closure history.
Attachments, supporting-evidence uploads, PDF reports, Excel data exports, and additional reporting features require a Premium subscription.