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    • Choose the CAPA Manager workflow closest to the problem you need to control.
    • Core CAPA workflows
      • CAPA softwareCloud CAPA management for investigation, corrective action, verification and closure.
      • Corrective actionManage corrective actions, NCRs, preventive actions and recurring quality issues.
      • 8D SoftwareGuide teams through containment, root cause analysis, RCCA and 8D reporting.
      • Audit actionTrack findings, assign owners and close audit corrective actions with evidence.
    • Specialist solutions
      • FRACASCapture failures, analyze causes and prevent recurrence in one controlled workflow.
      • EnvironmentalRecord environmental events, actions, evidence, approvals and follow-up tasks.
      • Health and safetyHandle incidents, hazards, actions and closure with traceable ownership.
      • Product Investigation SoftwareManage product investigations, PIR records, evidence and approvals.
      • Enterprise CAPABespoke CAPA Manager application services for private or managed server deployments.
    • Learn
      • What is CAPA software?A practical guide to CAPA systems, workflows and quality management terms.
      • CAPA Manager featuresExplore CAPA Manager 3 features for workflows, dashboards, reports, approvals and integrations.
  • Industries
    • Find pages relating to your industry.
    • Standards and sectors
      • PharmaSupport GMP-aligned deviation, CAPA and investigation workflows.
      • MedicalSupport ISO 13485 and FDA-regulated quality system requirements.
      • AerospaceSupport AS9100 quality teams with NCRs, supplier actions and 8D investigations.
      • AutomotiveSupport IATF 16949 teams with 8D, RCCA and action tracking.
      • Other industriesOperational issue management for energy, food, chemical and service teams.
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    • Useful services, templates and tools from our quality improvement work.
    • Services
      • Training servicesPractical training and improvement support for quality and operations teams.
      • Application developmentCustom software engineering for quality and operational workflows.
    • Templates and tools
      • 360 Degree feedbackA simple template for structured management and team feedback.
      • NPI Stage Gate templateA practical APQP and new product introduction gate review tool.
      • BOS ChartA business operating system chart template for performance tracking.
      • Gauge R&R MSAMeasurement system analysis support for repeatability and reproducibility.
      • Free quality toolsTemplates, calculators and practical resources for improvement teams.
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      • Contact usTalk with our team about CAPA Manager, pricing or implementation questions.
      • Free CAPA accountCreate a trial account and start using CAPA Manager.
      • User guideRead the CAPA Manager user guide and product instructions.
      • FAQsAnswers to common CAPA Manager and trial account questions.
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      • MediaShort product videos and CAPA Manager walkthroughs.
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      • Knowledge baseArticles about CAPA, RCA, 8D, quality systems and improvement.
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      • Terms of serviceService terms and usage conditions.
      • Subscriber AgreementSubscription agreement for CAPA Manager customers.
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      • Security profileSecurity, hosting and data protection information.
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CAPA Software Demo
Home
CAPA Software

Core CAPA workflows

  • CAPA software
  • Corrective action
  • 8D Software
  • Audit action

Specialist solutions

  • FRACAS
  • Environmental
  • Health and safety
  • Product Investigation Software
  • Enterprise CAPA

Learn

  • What is CAPA software?
  • CAPA Manager features
Industries

Standards and sectors

  • Pharma
  • Medical
  • Aerospace
  • Automotive
  • Other industries
Pricing
Other Products

Services

  • Training services
  • Application development

Templates and tools

  • 360 Degree feedback
  • NPI Stage Gate template
  • BOS Chart
  • Gauge R&R MSA
  • Free quality tools
More

Get started

  • Contact us
  • Free CAPA account
  • User guide
  • FAQs

Resources

  • CAPA Manager news
  • Media
  • Reviews
  • Knowledge base

Documents

  • Terms of service
  • Subscriber Agreement
  • Privacy statement
  • Security profile
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Supplier Corrective Action Software for 8D and SCAR

Supplier corrective action software for supplier quality teams

CAPA Manager helps manufacturers manage supplier corrective action requests, supplier 8D reports, SCAR workflows, root cause analysis, containment, corrective action plans, evidence, approvals, and verified closure in one cloud-based system.

Control supplier 8D and SCAR workflows

Assign investigations to internal owners and supplier contacts, track response status, collect evidence, and keep every decision attached to the corrective action record.

  • Supplier 8D reports and RCCA workflows
  • SCAR tracking with owners, due dates, and reminders
  • Root cause analysis using 5 Whys, Ishikawa, and structured 8D steps
  • Evidence attachments, approvals, and audit-ready history
  • Dashboards for overdue supplier actions and recurring issues

Supplier quality management software that links back to CAPA

When supplier issues affect production, customer complaints, incoming inspection, or audit findings, CAPA Manager keeps supplier action tracking connected to your wider corrective action software and CAPA management software process.

Start free supplier corrective action trial

What supplier 8D software should control

Supplier corrective action requests can lose momentum when information is split between email, spreadsheets, shared drives, and supplier portals. CAPA Manager gives teams a structured place to record the issue, capture containment, request supplier response, review root cause, approve action plans, and verify completion.

The same record can hold evidence, attachments, dates, decisions, reminders, and status changes. This makes it easier to brief purchasing, quality, engineering, production, and supplier contacts without rebuilding the story each time.

When to use supplier corrective action tracking

Use supplier 8D and SCAR workflows for incoming inspection failures, late or incomplete corrective action responses, customer-impacting supplier defects, repeated delivery issues, audit findings, warranty themes, and process escapes that need formal closure.

Review supplier performance trends

Supplier corrective action records become more valuable when teams review them together. Look for repeated defect types, late responses, weak root causes, incomplete evidence, and actions that do not prevent recurrence. These patterns can guide supplier development, purchasing decisions, audit planning, and incoming inspection priorities.

CAPA Manager helps preserve that history so future supplier discussions are based on evidence rather than memory.

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Adaptive Business Management Systems Ltd. is a company registered in England and Wales.

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