ISO/IEC 27003:2017
Improvement – ISO/IEC 27003:2017

ISO/IEC 27003:2017 ISO27003-10.1: Nonconformity and corrective action

When a nonconformity arises, respond to it by containing and correcting it and handling its consequences where applicable; decide whether its causes must be removed so it neither returns nor appears elsewhere, by reviewing it, finding its causes and checking whether similar cases exist or could arise; take whatever action is needed; check that corrective action worked; change the ISMS if that is necessary; keep corrective action proportionate to the effect of the nonconformity; and keep documented evidence of what the nonconformity was, what was done and the outcome. Implementation points (general practice; the 27003 guidance text is not held): nonconformities come from audits, monitoring, incidents and complaints; correct first, then remove the cause and verify later.

Maintained by Gerard BlokdykControl text last updated

What else in your programme already covers this

This control maps to 50 controls across 44 other frameworks. If you already hold one of them, the evidence you collected for it is the starting point here rather than new work.

  • IEC62304-4.1 Quality Management System
  • IEC62304-9.6 Analyze Problems for Trends
  • ISO-17025-8.1 Options
  • ISO-17025-8.7 Corrective actions
  • NFPA1600-7.2 After-Action Reporting
  • NFPA1600-8.2 Corrective Action
  • AS9100D-10.2 Nonconformity and Corrective Action
  • ACQS-8-3 Continuous Improvement
  • DIQ-2 Data Quality Management
  • IS.AR.210 Findings and Corrective Actions

ISO 10006:2003 · 1 control

  • 8.3 Continual improvement

ISO 14001:2015 · 1 control

  • 10.3 Continual improvement

ISO 14004:2016 · 1 control

  • 10.3 Continual improvement
  • ISO-14064-1-8 Quality management of the GHG inventory
  • ISO-20400-6.5 Monitoring and continuous improvement

ISO 22000:2018 · 1 control

  • 10.2 Continual improvement

ISO 22301:2019 · 1 control

  • 10.1 Nonconformity and corrective action

ISO 27005:2022 · 1 control

  • 10.8 Continual improvement

ISO 27701:2019 · 1 control

  • 5.8.2 Continual improvement

ISO 30401 · 1 control

  • ISO30401-15 Nonconformity and corrective action

ISO 31000:2018 · 1 control

  • 4.h Continual improvement

ISO 37001:2016 · 1 control

  • 10.2 10.2 Continual improvement

ISO 37301:2021 · 1 control

  • 10.1 Continual improvement
  • ISO-39001-10.1 Nonconformity and corrective action
  • ISO-41001-10.1 Nonconformity and corrective action

ISO 45001:2018 · 1 control

  • 10.3 Continual improvement
  • 10.2 Continual improvement

ISO 55001:2014 · 1 control

  • 10.3 Continual improvement

ISO 56002 · 1 control

  • ISO-56002-10.2 Deviation, nonconformity and corrective action

ISO 9001:2015 · 1 control

  • 10.3 Continual improvement

ISO/IEC 23894:2023 · 1 control

  • ISO23894-4.8 Continual Improvement

ISO/IEC 27014:2020 · 1 control

  • 27014-5.6 Continuous improvement

ISO/IEC 42001:2023 · 1 control

  • 10.1 Continual improvement
  • ITAR-CompliancProgram-ICP-EmpoweredOfficial-Recordkeeping-5Years-Training-IT-Cloud-SupplyChain-Coord-EAR-OFAC-Wassenaar ITAR Compliance Program + Internal Compliance Program (ICP) + Empowered Official + 5-Year Recordkeeping + Training + IT/Cloud (GovCloud + Azure Gov + GCC High) + Supply Chain + Coord EAR + OFAC + Wassenaar + MTCR

NIST SP 800-30 · 1 control

  • NISTSP30-8 Risk Assessment Maintenance, Continuous Monitoring, and Integration with the RMF

NIST SP 800-37 · 1 control

  • NISTSP37-7 RMF Monitor Step: Continuous Monitoring and Ongoing Authorisation

NIST SP 800-39 · 1 control

  • NISTSP39-5 Risk Monitoring: Effectiveness, Changes, Compliance, and Reassessment Triggers
  • PICSGMP-1 Chapter 1: Pharmaceutical Quality System (PQS) and Quality Risk Management
  • SAEIGHT-7 Management System, Worker Engagement, Continuous Improvement
  • 2.5.2 Verification Activities

South Korea ISMS-P · 1 control

  • ISMSP-MS-04 Management Review and Improvement
  • UKOPRES-5 Third-Party Risk, Concentration Risk

Every mapping shown was judged rather than inferred from wording similarity, and the ones that failed review are published too. See the coverage reports and what was rejected.

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