From an ongoing discussion in the ISO Standards Discussion listserve. Food for thought.
--------------------
From: ISO Standards Discussion
Date: Tue, 16 May 2000 18:31:26 -0500
Subject: Re: ISO 2000 impact /Briggs/Hankwitz/Vianna
From: "Vianna, Sidney"
John, as usual, very well said.
To expect Registrars to be the measure of product performance and system effectiveness, is not realistic. How many days, in average, does a third-party auditor spend in certified companies/ year? 2, 3, 4???
If users of third-party certificates wanted Registrars to be accountable for such issues, we ( Registrars) would need to spend way more time that we presently spend at certified companies.
Compliance with Management International Standards does not guarantee either product performance (which is clearly stipulated/commented in the ISO 9001 Standard) nor system effectiveness. If compliance with ISO 9000, guaranteed system effectiveness, our UK colleagues would dominate the World Economy, because, relatively speaking, the number of certified organizations is dramatically higher in the UK, compared to any other region in the World. We know this not to be the case.
Concerning the question:
> Has a registrar ever been sued for misrepresenting a company as
> having an effective quality management system?
I do not believe so. By design, Registrars verify COMPLIANCE of the system to a set of requirements. NOT effectiveness.
I would welcome a discussion about making Registrars more accountable for the effectiveness of the certified company's quality system. However, we would need a whole set of new rules for that game. The current accreditation's rules does not provide for this expectation.
What can a third-party auditor do if an organization chooses to have a MRB process with 15 required signatures to disposition non-conforming product, rather than 1 or 2? What can a third party auditor do, if design reviews, although conducted, are totally meaningless because the few organizational interfaces identified did not have qualifications or competence to provide meaningful feedback at that stage of the design?
Opportunities for improvement. That is all third-party auditors can offer. Few organizations pay attention to that.
Instead of complaining about millions of dollars that might have been wasted in certifications, I would be concerned with the BILLIONS of dollars that have been wasted in IMPLEMENTING ISO 9000 compliant systems that are totally inadequate. Unfortunately, there are so many organizations out there that do not realize the importance of aligning their quality system with their business practices. Until organizations understand that quality is a mind set, rather than a department, we will have an uphill battle.
PS In addition to the information you provided about the suspension, by the RvA, of a major Registrar, there is another large Registrar, operating in the US that has their Scope of Accreditation partially suspended, also by the RvA. This information is available in the RvA website, but one must dig, before one finds it.
Best regards,
Sidney Vianna
--------------------
From: ISO Standards Discussion
Date: Tue, 16 May 2000 18:31:26 -0500
Subject: Re: ISO 2000 impact /Briggs/Hankwitz/Vianna
From: "Vianna, Sidney"
John, as usual, very well said.
To expect Registrars to be the measure of product performance and system effectiveness, is not realistic. How many days, in average, does a third-party auditor spend in certified companies/ year? 2, 3, 4???
If users of third-party certificates wanted Registrars to be accountable for such issues, we ( Registrars) would need to spend way more time that we presently spend at certified companies.
Compliance with Management International Standards does not guarantee either product performance (which is clearly stipulated/commented in the ISO 9001 Standard) nor system effectiveness. If compliance with ISO 9000, guaranteed system effectiveness, our UK colleagues would dominate the World Economy, because, relatively speaking, the number of certified organizations is dramatically higher in the UK, compared to any other region in the World. We know this not to be the case.
Concerning the question:
> Has a registrar ever been sued for misrepresenting a company as
> having an effective quality management system?
I do not believe so. By design, Registrars verify COMPLIANCE of the system to a set of requirements. NOT effectiveness.
I would welcome a discussion about making Registrars more accountable for the effectiveness of the certified company's quality system. However, we would need a whole set of new rules for that game. The current accreditation's rules does not provide for this expectation.
What can a third-party auditor do if an organization chooses to have a MRB process with 15 required signatures to disposition non-conforming product, rather than 1 or 2? What can a third party auditor do, if design reviews, although conducted, are totally meaningless because the few organizational interfaces identified did not have qualifications or competence to provide meaningful feedback at that stage of the design?
Opportunities for improvement. That is all third-party auditors can offer. Few organizations pay attention to that.
Instead of complaining about millions of dollars that might have been wasted in certifications, I would be concerned with the BILLIONS of dollars that have been wasted in IMPLEMENTING ISO 9000 compliant systems that are totally inadequate. Unfortunately, there are so many organizations out there that do not realize the importance of aligning their quality system with their business practices. Until organizations understand that quality is a mind set, rather than a department, we will have an uphill battle.
PS In addition to the information you provided about the suspension, by the RvA, of a major Registrar, there is another large Registrar, operating in the US that has their Scope of Accreditation partially suspended, also by the RvA. This information is available in the RvA website, but one must dig, before one finds it.
Best regards,
Sidney Vianna