Split from ISO 10007 - Configuration Management Requirements by request.
ISO10007 gives guidelines to ensure that a complex product continues to function when components are changed individually. Since we are not a design responsible organization, our procedures will address configuration management only as pertains to us - such as change control and document control.
But the standard specifically requires:
AS9100 - 4.3 Configuration Management: The organizatioin shall establish, document and maintain a configuration management process appropriate to the product.
What do I do? Can I just put a couple of sentences in our policy manual that direct the reader to the various procedures that address configuration management stuff?
Or - because of the requirement to clearly show the relationship between our documented procedures and requirements in the standard, I've added a column to my list of Level II procedures where I've x-referenced the AS elements - I've already got 4.3 noted next to our procedures for Advanced Product Quality Planning, Contract Review, Control of Engineering Drawings, Control of Customer Specific Requirements and Preservation of Product. Think I could just leave it like that?
I do not want to write a procedure specifically for Configuration Management - it's not really its own process here. It's a part of many processes.
Well, I'm glad I did a search. I forgot I posted this last year - I almost started a new thread asking exactly the same thing. Anyway - Here's what I think:Cari Spears said:We manufacture products in accordance with someone else's configuration management plan - we're not design responsible. So I think our procedures need to address cmp's as they pertain to us - like change control/contract review and document control, etc. In the same manner that we control and use technical orders and repair manuals given to us by some of our customers (customer specific requirements).
I'm also not sure about configuration audits - who does them? The design responsible function who created the CMP? Or is it our final product inspection? 10007 says "A CA may be required for the formal acceptance of a configuration item."
ISO10007 gives guidelines to ensure that a complex product continues to function when components are changed individually. Since we are not a design responsible organization, our procedures will address configuration management only as pertains to us - such as change control and document control.
But the standard specifically requires:
AS9100 - 4.3 Configuration Management: The organizatioin shall establish, document and maintain a configuration management process appropriate to the product.
What do I do? Can I just put a couple of sentences in our policy manual that direct the reader to the various procedures that address configuration management stuff?
Or - because of the requirement to clearly show the relationship between our documented procedures and requirements in the standard, I've added a column to my list of Level II procedures where I've x-referenced the AS elements - I've already got 4.3 noted next to our procedures for Advanced Product Quality Planning, Contract Review, Control of Engineering Drawings, Control of Customer Specific Requirements and Preservation of Product. Think I could just leave it like that?
I do not want to write a procedure specifically for Configuration Management - it's not really its own process here. It's a part of many processes.
Last edited: