If you are referring to the
Phase 2 Revision to AS 9100 Rev C thread that you started, you clearly stated a revision to AS9100 was in the works, which, as I replied in the thread, is years away. I clearly said (and it is on the record) that a revision to AS9101 was likely and is forthcoming. The 9101 group met in New Orleans during the last IAQG meeting and a revision is underway. You are committing the mistake of making this personal. I come here to exchange ideas, opinions and facts. It just so happens that I have been a member of the AAQG for a decade now and a member of the Leadership Team for a couple. So, I do see first hand the deliberations and the good intentions behind many of the changes. However, I have been in the management system conformity assessment business for over 20 years and I also know the mindset of MANY (not all) CB auditors that will DELIBERATELY refuse to change their ways, despite training, feedback, write-ups, etc...Many (not all) auditors working for CB's don't believe rules should apply to them, don't like to be questioned about their knowledge and (God forbid) their interpretations. Case in point: Why there are so many organizations out there scrambling to identify their QMS processes and explain how they monitor them? That has been a requirement of ISO 9001 since the 3rd Edition, published over 10 years ago. Why do we have requirements in the standard that are totally neglected and auditors never write them up? Simply because the auditor does not understand the requirement either.
When AS9100B (ISO 9001:2000-based) came about, there was a statistical analysis of the non-conformities being written up against that version of the standard and compared against the AS9100A (ISO 9001:1994-based) write-ups. Some people reached a conclusion that organizations were failing to move away from the elemental approach of a QMS to a process-based approach. My conclusion was different; in my estimation, the write ups were similar simply because AUDITORS will stick to their comfort zone. After all is so much easier to find obsolete documents being used, gages with expired calibration being used, a stamp missing on a traveler, etc...Where are the gutsy auditors that are courageous and competent enough to issue non-conformities against top management for disregarding customer feedback and failing to provide resources? They are a minority in the ICOP process. Unfortunately, the criteria for one to become an AEA allowed too many people who worked 3 or 4 decades in quality control to qualify as an auditor. Not their fault, but many of them will NEVER understand the big Q and big M in QMS. They are uncomfortable auditing outside of the shop floor. So, AS9101D and the associated AATT is an attempt to make it clear that high-performance, added-value audits have to be done in different way.
I will respond to the well thought out paper Bradley posted on another thread soon, but please don't take my feedback as personal response. At least is not intended that way.
I come here to keep the perspective about the ICOP Scheme "fair and balanced".