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AS9100, AS9110 & AS9120 Aerospace and Defence Standards 2016

29th February 2016

The IAQG have advised that the revised standards are due for publication in April 2016 and the deadline for transition has been aligned with the revised ISO 9001:2015.  This means that there will not be a three-year transition period but rather two years and five months.  Any organisation not transitioning successfully before the deadline will be de-registered automatically.

All certificate holders are advised to plan for the new standards and ensure that they are aware of the changes and timescales.

We will plan the transition with our Clients as soon as the publication has been made.

Just to remind readers:

The revised standards use the Hi Level Annex SL format produced for all new ISO standards and comprise ten clauses.

  1. Scope
  2. Normative references
  3. Terms and definitions
  4. Context of the organisation
  5. Leadership
  6. Planning
  7. Support
  8. Operation
  9. Performance evaluation
  10. Improvement

A number of the requirements deemed unnecessary in ISO 9001:2015 have been reinstated in AS 9100.

These additional requirements are necessary for control and traceability required in the aerospace industry, which would not be met with the basic ISO9001 standard.

These include:

  • management representative is required
  • documented information with items to be identified (Quality Manual)

In addition, a number of requirements have been added:

  • Protection from counterfeit products, 
  • Product safety (awareness and compliance)
  • Computer back up secured
  • Project management
  • Measures of on-quality and on-time delivery
  • Stakeholders
  • Transfer of work
  • Reviews of requirements related to products and services coordinated with applicable  functions
  • Actions to be taken when not meeting customer requirements
  • Handling obsolescence
  • Changes
  • Controls of external providers and sub-tier providers
  • Additional evaluation of data and test reports
  • Controls of production equipment
  • Tools and software programmes
  • Validation of special processes
  • production process variations
  • problems detected after delivery
  • procedure to define NC process and responsibilities
  • review of on-time delivery performance
  • actions based on risk assessments, and human factors.
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