IA9100 Clause-by-Clause Changes from AS9100D
This page sets out, clause by clause, how the IA9100 draft changes compared with AS9100D, based on the IAQG key change summary. Use it to scope a gap assessment, then read the deeper guides on operational planning (clause 8.1) and counterfeit parts prevention.
Significant changes at a glance

Cultural focus
Organizational culture and ethical behaviour are now emphasized as essential to an effective QMS (clauses 0.1, 5.1 and 7.1.4).

Information security
A new clause 7.1.7 requires you to plan, implement and control information security to safeguard the QMS.

Safety and prevention
Product safety (8.1.3) and counterfeit parts prevention (8.1.4) notes become explicit requirements.
Clause-by-clause summary table
| Section | Clause | Change | What changes |
|---|---|---|---|
| Introduction | 0.1 General | Enhanced | Importance of organizational culture and ethical behaviour to an effective QMS and its ability to achieve intended results. |
| Introduction | 0.2 Quality management principles | Enhanced | Implementation of the QMS is a cornerstone to establishing a culture of quality. |
| Terms | 3 Terms and definitions | Clarified | Examples of software and electronic devices added to “modified part”. |
| Context | 4.1–4.3 | No change | — |
| Context | 4.4 QMS and its processes | Clarified | NOTE clarifies that identifying processes is an organizational decision. |
| Leadership | 5.1 Leadership and commitment | Enhanced | Leadership ensures quality-culture goals and objectives are consistent with policy, vision, mission, values and context, and promotes an ethical work environment. |
| Leadership | 5.2–5.3 | No change | — |
| Planning | 6.1 Risks and opportunities | Clarified | NOTE clarifies operational risk controls in clause 8.1.1. |
| Planning | 6.2–6.3 | No change | — |
| Support | 7.1.1–7.1.3 | No change | — |
| Support | 7.1.4 Environment for the operation of processes | Enhanced | Culture added as an example in the NOTE on human and physical factors: quality, ethical behaviour, product and personnel safety, quality of work life. |
| Support | 7.1.5 Monitoring and measuring resources | Enhanced | Measurement system analysis (MSA) introduced in a NOTE for analysing variation; lists of monitoring and measuring equipment kept as documented information (for example, a register). |
| Support | 7.1.6 Organizational knowledge | No change | — |
| Support | 7.1.7 Information security | New | New requirement for information security to safeguard the QMS so it achieves its intended results. |
| Support | 7.2–7.5.2 | No change | — |
| Support | 7.5.3 Control of documented information | Clarified | Further refined requirements when documented information is managed electronically. |
| Operation | 8.1 Operational planning and control | Enhanced | Information security and data protection added to the NOTE; MSA and control plans added; operations to prevent, detect and mitigate foreign object debris (FOD); APQP named as one method. |
| Operation | 8.1.1–8.1.2 | No change | — |
| Operation | 8.1.3 Product safety | Enhanced | NOTE items become requirements: hazard identification, safety risks, change impact, safety process effectiveness, training, communication and awareness, and event reporting. |
| Operation | 8.1.4 Prevention of counterfeit parts | Enhanced | NOTE items become requirements: training, parts obsolescence monitoring, traceability, test methods, monitoring external reports, and segregation, containment and reporting. |
| Operation | 8.2 Requirements for products and services | No change | — |
| Operation | 8.3.2 Design and development planning | Clarified | Clarifies dividing design and development into distinct activities. |
| Operation | 8.3 (other sub-clauses) | No change | — |
| Operation | 8.4.2 Type and extent of control | Clarified | NOTE updated to allow remote inspection and audit of external providers. |
| Operation | 8.4.3 Information for external providers | Enhanced | Restructured for clarity, adding determination of the level of control over direct and sub-tier external providers. |
| Operation | 8.5.1 Control of production and service provision | Clarified | The 8.5.1.d NOTE is clarified and aligned with 8.5.1.1. |
| Operation | 8.5.1.3 Production process verification | Clarified | Structure changed to make clear that production process verification is more than first article inspection (FAI). |
| Operation | 8.5.2–8.7 | No change | — |
| Performance evaluation | 9.1, 9.3 | No change | — |
| Performance evaluation | 9.2 Internal audit | Enhanced | Reviewing performance indicators changes from a NOTE to a requirement; risks must be included when establishing the audit program. |
| Improvement | 10.1–10.2 | No change | — |
| Improvement | 10.3 Continual improvement | Enhanced | Plan periodic QMS maturity assessments and set improvement goals and objectives. |
Culture and leadership (0.1, 5.1, 7.1.4)
Monitoring and measurement (7.1.5)
Information security (7.1.7 and 8.1)
Operational planning (8.1)
Product safety (8.1.3)
Counterfeit parts prevention (8.1.4)
The counterfeit parts NOTE items become requirements covering training, obsolescence monitoring, approved sources, traceability, test methods, external reporting, and segregation and containment. See the IA9100 clause 8.1.4 requirements on our counterfeit parts guide.
External providers (8.4.2, 8.4.3)
Production (8.5.1, 8.5.1.3)
Internal audit and improvement (9.2, 10.3)
Timeline
- 2021–2024Development and draftingIA9100 revision drafted, with industry comments integrated.
- Late 2026Expected publicationAnticipated Q4 2026 release of the IA9100 standard.
- 1 January 2027Audits expected to beginAnticipated start date for audits against the new standard.
- 2026–2029Transition periodAn anticipated three-year window to migrate from AS9100 to IA9100.
Estimates only; the IAQG is the authority on publication and transition dates. Ready to act? See our step-by-step transition guide or book an IA9100 gap assessment.











