IAQG 9101:2016 (Rev F)

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IAQG 9101:2016 (Rev F) Changes Overview Prepared by the IAQG 9101 team 16 November 2016

Presentation Objectives Part One: Overview of 9101:2016 (Rev F) Team Membership Team Coverage Stakeholders Key Reasons for Change Key Revision Summary Revision Schedule Part Two: Key Revision Detail 9101:2016 (Rev F) Standard Part Three: Key Revision Detail 9101:2016 (Rev F) Forms 2

Part One Overview of 9101:2016 (Rev F) 3

9101 Team Membership (Until 12 Oct. 2016) Masahiro Kawamoto 9101 IDR Team Leader Mitsubishi Heavy Industries Brian Geer Conny Flink Masahiro Kawamoto 9101 AAQG SDR Lockheed Martin 9101 EAQG SDR GKN Aerospace Engine Systems 9101 APAQG SDR Mitsubishi Heavy Industries Tom Gallagher Wilfried Weber 9101 AAQG Representative United Technologies Corporation 9101 EAQG Representative PFW Aero Alain Bonnel Stuart Anthony 9101 EAQG Representative SAFRAN 9101 Scribe IAQG Bob Keys 9101 CB Representative DNV GL Emeritus Mark Heaton-Watts 9101 EAQG Representative Rolls-Royce Paul Dionne 9101 CB Representative ABS-QE Insert Picture Here Michel Jacquaniello 9101 EAQG Representative Zodiac Aerospace Francois Dumesnil 9101 CB Representative Bureau Veritas Gary Procter 9101 CB Representative LRQA 4

9101 Team Coverage 13 members on the 9101 Team Representing: Americas, Europe, and Asia-Pacific IAQG sectors 8 IAQG member companies 6 Different countries 4 Certification Body members 1 Dedicated Scribe 5

9101 Stakeholders Aviation, Space and Defense supply chain IAQG member companies IAQG community and working groups Accreditation and Certification Bodies AQMS auditors Aviation, Space and Defense authorities 6

9101 Key Reasons for Change Publication of ISO17021-1:2015, ISO9001:2015 and 9100 series:2016 standards FAQs arising from 9101:2014 (Rev E) OASIS feedback requests Stakeholder feedback Lessons learned from OPMT oversight of CB audit reports Support of the OASIS Next Generation (NextGen) project 7

Key Revision Summary Incorporated updated requirements and revised terminology from new revisions of ISO9001:2015, ISO17021-1:2015 and 9100 series:2016 standards Changed PEAR application from previous 9100-series clause 7 (Product Realization) to new 9100-series clause 8 (Operation) Changed process effectiveness levels from 4 to 5 and simplified Process Evaluation Matrix (PEM) definitions Clarified raising of NCRs in relation to nonconformities Audit approaches moved from the 9101 standard into Auditor Guidance Material Simplified the content of 9101 clauses relating to Stage 1 audit to align with changes to Form 1 Simplified/clarified Form entries and instructions to support audit reporting using OASIS NextGen 8

9101:2016 Revision Schedule 2014 2015 Long Beach 10/2014 Chengdu 04/2015 Charlotte, NC 08/2015 Madrid 10/2015 Trollhattan, SE 03/2016 Singapore 04/2016 2016 Derby UK 06/2016 Miami 10/2016 2017 Stockholm 04/2017 9100 Final Draft Launch 9101 Revision Team Working Draft Coordination Draft CD Comments Review Ballot Draft Ballot Comments Ballot Review Comments Final Draft 9101 Publication (AS, pren, SJAC) ISO 17021-1 FDIS Incorporation ISO 17021-1 Publication 9101 Revision Schedule - Working Draft: May 2015 - Coord. Draft (30 days): Aug. 2015 - CD Comments Review: Oct. 2015 - Ballot Draft: Nov. 2015 - BD Comments Review : Mar. 2016 - IAQG Final Draft for publication : Jun. 2016-9101:2016/Rev. F Publication: Oct. 2016 (AS, pren, SJAC standards) Complete Not complete IAQG Face to Face Meeting Additional 9101 Face to Face Team Meeting ISO/IEC 17021-1 Schedule - FDIS Voting: 5 March - 5 May 2015-17021-1:2015 Publish: July 2015 9

Part Two Update to 9101 Standard 10

Updated Major / Minor nonconformity definitions (clauses 3.3 and 3.4) ISO17021-1:2015 definitions have been linked as a requirement Additional 9101 definitions continue to be included Rationale: Definitions rationalized to include each respective definition from ISO17021-1 11

Removed Audit Approaches [9101:2014 (Rev E) clause 4.1.2] Requirements for using specific Audit Approaches moved into updated 9101:2016 (Rev F) Auditor Guidance Material. Requirements for conducting an audit of Special Processes has been moved to clause 4.2.2.4.1 Rationale: To build upon the maturity developed by auditors in their approach towards conducting process based audits, and to provide additional flexibility in the audit approach Special process audit requirements was part of audit approaches and since those have been moved into guidance material the need to retain specific requirements has been relocated 12

Clarified audit reporting requirements (clause 4.1.2) Updated to allow the recording of process information into one QMS Process Matrix Report Table 1 updated to align Special audit reporting with other audit phases Note added to Table 1 to provide guidance on the use of Forms 2 and 3 for Special audits Rationale: To provide more flexibility when common processes exist across multiple sites, campus, several sites or complex organization To provide a more unified audit reporting approach for all audit phases Note added to show that the reason for a special audit (clause 4.3.6) may have an impact on the use of Forms 2 and 3 13

Clarified the issuing of NCRs relating to Operational processes (9100-series clause 8): Process Results (clause 4.2.2.5.1): The audit team shall issue an NCR against the relevant 9100-series standard clause when the process is not delivering the planned results and appropriate action is not being taken Process Realization (clause 4.2.2.5.2): The audit team shall issue an NCR against the relevant 9100-series standard clause when planned activities of a process are not realized, or not fully realized Rationale: To emphasize the requirement when to issue NCRs in relation to Process Results and Process Realization..see diagram on next page 14

Audit of Operational processes (9100-series clause 8) 9101 clause 4.2.2.5.1 Record process performance results on the PEAR (Section 2) Issue an NCR when the process is not delivering the planned results and appropriate action is not being taken Record process realization results on the PEAR (Section 3) Issue an NCR when planned activities of a process are not realized or not fully realized 9101 clause 4.2.2.5.2 Evaluate the audit evidence from the PEAR and select the corresponding effectiveness value from the PEM 9101 clause 4.2.2.5.3 15

Audit findings and resultant effectiveness level NCR(s) have not been issued NCR(s) have been issued related to Process Realization NCR(s) have been issued related to Process Results NCR(s) have been issued related to Process Realization and Process Results Reminder The process effectiveness level is determined from the audit results (conformity and nonconformity) 16

Updated PEM (clause 4.2.2.5.3 Table 3) Simplified Process Realization wording defined and implemented becomes determined Assessment levels revised from 4 to 5 and redistributed within the matrix Rationale: To align the text with 9100-series terminology To provide more balance relating to the effectiveness result To improve the visual representation of process risk 17

Level 2 here means that the process is determined and planned activities are partly or fully realized. The process however is not delivering the planned results and appropriate action is not being taken. Updated PEM Assessment Levels 1 & 2 Level 1 means that the process is not determined and planned activities are not realized. Furthermore the process is not delivering the planned results and appropriate action is not being taken. Level 2 here means that the process is not determined and planned activities are not realized. The process however is delivering the planned results or if not, appropriate action is being taken. 18

Updated PEM Assessment Levels 3 & 4 Level 4 here means that the process is determined and planned activities are fully realized. The process however is not delivering the planned results but appropriate action is being taken. Level 3 means that the process is determined but planned activities are not fully realized. The process however is not delivering the planned results but appropriate action is being taken. Level 4 here means that the process is determined but planned activities are not fully realized. The process however is delivering the planned results. 19

Updated PEM Assessment Level 5 Level 5 means that the process is determined and planned activities are fully realized. Furthermore the process is delivering the planned results. 20

Clarified the requirement for the audit team leader to provide the organization with applicable NCR(s) and PEAR(s) associated with those NCRs (clause 4.2.2.7) Rationale: To show that only PEARs associated with the respective NCR(s) need to be provided at the closing meeting 21

Removed the requirement to issue a separate audit report for integrated audits (clause 4.2.3) Rationale: Allow a single report for integrated audits by indicating Yes/No on Forms 5 and 6 The requirement for separate reports for a combined audit is retained in accordance with IAQG OPMT ICOP Resolutions Log #105 22

New requirement to verify the effectiveness of corrective actions taken for nonconformities (if applicable) identified during the previous audit (clauses 4.3.4 and 4.3.5) Rationale: To strengthen the verification of corrective action effectiveness during subsequent audits (if applicable) and to align with a new requirement in ISO17021-1 clause 9.4.8.2 r 23

Clarified the reasons for conducting a Special Audit (clause 4.3.6 a & b) An organization s request to revise their existing: Certification scope Certification structure Number of site(s) and/or location(s) Transfer of certification from one CB to another (see 9104/1 clause 8.8) Rationale: To accommodate other reasons for conducting a Special Audit, in particular an increase or reduction to the certification scope, certification structure, number of sites or number of locations 24

Part Three Update to 9101 Forms Form 1 Form 2 Form 3 Form 4 Form 5 Form 6 25

Form 1 (Stage 1 Audit Report): Exclusions box changed to Requirements determined as not applicable, Justification box added and Quality Manual changed to QMS Documented Information Key Requirements replaced with Confirmation of Requirements and now includes 9100-series clause numbers & titles Key Information reduced in scope and renamed Other Information Removed Website and Subsidiary of boxes NOTE added to instructions to allow the use of attachments..continued 26

Form 1 (Stage 1 Audit Report) continued: Disclaimer statement added Rationale: To align with updated 9101 & ISO17021-1 requirements and 9100-series clauses and terminology To provide more consistency when confirming requirements against the 9100-series standards To support OASIS NextGen 27

Form 2 (QMS Process Matrix Report): 9100-series clause numbers & titles changed Clarified when N/A and empty boxes can be utilized in populating the matrix Changed to accommodate Summary of Objective Evidence for 9100-series clauses 4,5,6,7,9 and 10 Changed to accommodate reporting (5) PEAR levels Changed to identify common process application across multiple sites, campus, several sites or complex organizations NOTE added to instructions to allow the use of attachments..continued 28

Form 2 (QMS Process Matrix Report) continued: Disclaimer statement added Rationale: To align with updated 9101 & ISO17021-1 requirements and 9100-series clauses and terminology To allow one report when common processes exist across multiple sites, campus, several sites or complex organizations To support OASIS NextGen 29

Form 3 (PEAR): Added the box Responsibility/Authority for the process Assessment levels revised from 4 to 5 and redistributed Updated the PEM image NOTE added to instructions to allow the use of attachments Disclaimer statement added Rationale: To align with updated 9101 & ISO17021-1 requirements and 9100-series terminology To provide more balance in relation to the effectiveness result To help with PEAR level determination when using the Form To support OASIS NextGen 30

Form 4 (NCR): Added Cause Code box Deleted Signature boxes NOTE added to instructions allowing the use of attachments Disclaimer statement added Rationale: To align with updated ISO17021-1 requirements To accommodate the allocation of a suitable Cause Code from the IAQG listing in order to support future data collection. To support OASIS NextGen 31

Form 5 (Audit Report): Audit type expanded to include reason for Special Audit Removed Website and Subsidiary of boxes Box added to signify Integrated Audit (Yes/No) Exclusions box changed to Requirements determined as not applicable, Justification box added and Quality Manual changed to QMS Documented Information Changed to accommodate reporting (5) PEAR levels Inclusion of a statement to verify the effectiveness of corrective actions taken for nonconformities identified during the previous audit..continued 32

Form 5 (Audit Report) continued: Clarified statement for the audit team leader s certification recommendation Deleted Signature boxes NOTE added to instructions allowing the use of attachments Disclaimer statement added Rationale: To align with updated 9101 & ISO17021-1 requirements and 9100-series terminology To provide more consistency when recommending the certification decision To support OASIS NextGen 33

Form 6 (Supplemental Audit Report): Audit type expanded to include reason for Special Audit Changed to accommodate reporting (5) PEAR levels Deleted Signature boxes Box added to signify Integrated Audit (Yes/No) NOTE added to instructions to allow the use of attachments Disclaimer statement added Rationale: To align with updated 9101 & ISO17021-1 requirements and 9100-series terminology To support OASIS NextGen 34

Forms continue to be referenced in Appendix B Electronic versions of the Forms will remain accessible via the IAQG website together with supporting instructions. http://www.sae.org/iaqg/ 35