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    • Choose the CAPA Manager workflow closest to the problem you need to control.
    • Core workflows
      • CAPA softwareCloud CAPA management for investigation, corrective action, verification and closure.
      • Corrective actionManage corrective actions, NCRs, preventive actions and recurring quality issues.
      • Audit actionTrack findings, assign owners and close audit corrective actions with evidence.
    • Investigation 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 CAPACustom 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.
    • Also useful
      • 8D SoftwareGuide teams through containment, root cause analysis, RCCA and 8D reporting.
      • Supplier corrective action
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    • Find pages relating to your industry.
    • Standards and sectors
      • PharmaSupport GMP aligned deviation, CAPA and investigation workflows.
      • MedicalSupport structured medical device CAPA and ISO 13485 quality processes.
      • 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 tasks.
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      • Contact usCAPA Manager sales and support.
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Home
CAPA Software

Core workflows

  • CAPA software
  • Corrective action
  • Audit action

Investigation solutions

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

Learn

  • What is CAPA software?
  • CAPA Manager features

Also useful

  • 8D Software
  • Supplier corrective action
Industries

Standards and sectors

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

Services

  • Training services
  • Application development

Templates and tools

  • Free quality tools
More

Get started

  • Contact us
  • Free CAPA Manager Account
  • User guide
  • FAQs

Resources

  • CAPA Manager news
  • Media
  • Reviews
  • Knowledge base

Documents

  • Terms of service
  • Subscriber Agreement
  • Privacy statement
  • Security profile

Raise a new investigation in CAPA Manager

Raise a new CAPA request, capture the initial problem statement, and start a corrective action investigation.

Using this video with your team

Choose a realistic but non-sensitive problem and gather the known facts before viewing. After the demonstration, ask each participant to draft the opening description in their own words and compare what information they included.

Pause at the problem statement, classification and assignment steps. Discuss the difference between an observed symptom and an assumed cause, and identify who should own the initial investigation in your organization.

Consider whether the opening record captures enough information to begin controlled work: what happened, where and when it was found, the known impact, any immediate response and the person responsible for investigating it.

Related resources

The root-cause analysis and CAPA features pages explain the structured tools available after an investigation is opened. Use the user guide when you need field-by-field operating instructions.

Enter the same sample problem twice: once as a vague statement and once using specific facts. Comparing the two records is a useful way to show why a clear starting description matters.

Evaluation checklist

Make sure occasional users can identify the required information, select an appropriate workflow and assign responsibility without guessing. Review whether your procedure needs any local guidance for categories, priorities or target dates.

Do not try to establish the root cause while raising the request; record what is known and leave investigation conclusions for the investigation stage.

One workflow at a time

Keep the first record factual and concise. A sound investigation starts with a problem statement that does not presume the answer.

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