SBS - The best value in QMS software

Reasons for the Decline of ISO 9001 Registrations in North America (circa 2010)

Elsmar Forum Sponsor

Sidney Vianna

Post Responsibly
Staff member
Admin
#72
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

I'd be very interested in knowing more about why you think a client wouldn't complain to their CB...
That is a good question, Andy. But, and unfortunately, many organizations are just interested in attaining and maintaining the certification. A competent CB auditor is secondary to the business need of keeping the certificate to appease a customer.

Many times, a bad auditor is "welcomed" simply because s/he is a known quantity. The bad auditor pretends to audit and issue non-conformities. The registrant "pretends" to do corrective action and the façade certification is maintained. Everyone is happy until a real problem happens and the registrant's customers demand answers....
 
Last edited:

Big Jim

Super Moderator
#73
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

That is a good question, Andy. But, and unfortunately, many organizations are just interested in attaining and maintaining the certification. A competent CB auditor is secondary to the business need of keeping the certificate to appease a customer.

Many times, a bad auditor is "welcomed" simply because s/he is a known quantity. The bad auditor pretends to audit and issue non-conformities. The registrant "pretends" to do corrective action and the façade certification is maintained. Everyone is happy until a real problem happens and the registrant's customers demand answers....
How true.
 

Big Jim

Super Moderator
#74
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

That may have been true in the days of the mantra "say what you do, do what you say" that someone at DuPont coined early on in the history of the rush to get certified in the USA...actually, ISO has NEVER been about "say what you do..." because it forces many organizations to put practices in place they never did before!

Today, the effectiveness of a system is not in the eye of the auditor! It is in the data management present as part of their review and conclusions of the suitability and effectiveness of their system!

Those who still cling to the mantra are well advised to get past that, or risk going the way of dinosaurs!
I don't remember the last time I used that phrase. Very early in my ISO experience I realized that it did not really reflect the standard. If anything, as you pointed out, it led to over documentation and tended to push toward perceiving the standard as being very company unfriendly.
 
Last edited:

howste

Thaumaturge
Super Moderator
#75
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

I recently spoke at an ASQ meeting, and at one point during some Q&A, I encouraged the attendees to let their certification bodies know if they had bad audit experiences, ineffective audits, or invalid nonconformities. There were quite a few people who said they were genuinely afraid of retaliation if they complained. To me this seems completely foreign. I make it a point to encourage feedback in both opening and closing meetings, and make sure that they are aware of the appeals process.

As has been said here many times before, this kind of feedback to the CBs is critical to improve the process and to educate or weed out poor performing auditors.
 
J

JaneB

#76
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

I recently spoke at an ASQ meeting, and at one point during some Q&A, I encouraged the attendees to let their certification bodies know if they had bad audit experiences, ineffective audits, or invalid nonconformities. There were quite a few people who said they were genuinely afraid of retaliation if they complained.
It's a very common belief/fear, however. On the (very few) occasions I've witnesses audits I believed merited being brought to the attention of the relevant manager at the CB, this was the very first thing they all mentioned: But won't it affect our audit? What if the auditor gets us back? What if... what if... etc

Yes, it's 'foreign' to us. But not to people who lack experience in the field.


To me this seems completely foreign. I make it a point to encourage feedback in both opening and closing meetings, and make sure that they are aware of the appeals process.
Some auditors here highlight the appeals process. It's a comparatively rare one who encourages any feedback at all on their audit. (They're the seriously good ones on the whole.)

As has been said here many times before, this kind of feedback to the CBs is critical to improve the process and to educate or weed out poor performing auditors.
Yes, it is. And on the (again, I emphasise very) rare occasion I have complained, the CB responded in a way that could not be faulted. On other occasions, I've given relatively informal feedback on an auditor who didn't suit, needed more experience, needed more client focus etc. Again, good results. And no, no 'comeback' for the client. Except improved service!
 

Wes Bucey

Prophet of Profit
#77
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

That is a good question, Andy. But, and unfortunately, many organizations are just interested in attaining and maintaining the certification. A competent CB auditor is secondary to the business need of keeping the certificate to appease a customer.

Many times, a bad auditor is "welcomed" simply because s/he is a known quantity. The bad auditor pretends to audit and issue non-conformities. The registrant "pretends" to do corrective action and the façade certification is maintained. Everyone is happy until a real problem happens and the registrant's customers demand answers....
Yep. Lots of folks would rather deal with the devil they know than one they don't.

I recently spoke at an ASQ meeting, and at one point during some Q&A, I encouraged the attendees to let their certification bodies know if they had bad audit experiences, ineffective audits, or invalid nonconformities. There were quite a few people who said they were genuinely afraid of retaliation if they complained. To me this seems completely foreign. I make it a point to encourage feedback in both opening and closing meetings, and make sure that they are aware of the appeals process.

As has been said here many times before, this kind of feedback to the CBs is critical to improve the process and to educate or weed out poor performing auditors.
As many will attest, Steve, not every auditor is as eager to throw a spotlight on the process. So, unless someone has you as the auditor or has heard you or someone like you speak at a business meeting (from any or all associations), they are not informed and FEAR (of losing a customer because of losing registration, of losing a job because of poor audit report, etc.) means they simply follow what Sidney has said above - "deal with the devil you know."
 
T

tyker

#78
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

Chances are, this was the same Certification Body that was taken to court in the UK several years ago for alleged misleading advertisement practices. If I remember correctly it was John Seddon who took them to court for advertising that ISO 9001 certification would lead to higher productivity, efficiency, profitability, etc...
I don't know who Seddon sued so can't comment on that but does it make any difference? Don't all the big CBs make the same claims these days?

Like a previous poster, if I were in need of a CB, I would be looking for one which provided a low cost, efficient auditing/certification service and that's all.

I know most CB auditors mean well. I know there are many clever, hard working CB auditors. But when it comes to business improvement I want advice from someone with a track record of implementing improvement, not just someone who's seen others do it.

Perhaps the CBs are simply moving away from their natural market.
 
#79
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

Like a previous poster, if I were in need of a CB, I would be looking for one which provided a low cost, efficient auditing/certification service and that's all.
This is an oxy-moron. Those CBs who are low(est) cost often employ staff who won't be equipped to do what you describe! I'm sure you mean 'reasonable cost', since there are many factors at play which affect the prices charged. In general terms, those which lead to the lowest cost - auditor pay, number of audit days etc adversely affect the outcome of the audit, credibility of certification etc.
 
T

tyker

#80
Re: What are the Reasons for the Decline of ISO 9001 Registrations in North America?

This is an oxy-moron. Those CBs who are low(est) cost often employ staff who won't be equipped to do what you describe! I'm sure you mean 'reasonable cost', since there are many factors at play which affect the prices charged. In general terms, those which lead to the lowest cost - auditor pay, number of audit days etc adversely affect the outcome of the audit, credibility of certification etc.
I don't agree. Low cost and efficient are natural partners and why would auditor pay affect the outcome of the audit? Lean principles dictate that I shouldn't pay for services I neither want nor need.
 
Thread starter Similar threads Forum Replies Date
L Reasons to submit a new PPAP or notify the customer APQP and PPAP 3
T Reasons to change certification body and typical costs Registrars and Notified Bodies 16
L Valid reasons to omit an "ear-tag" type label on a cable? IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
M Common Reasons for Out Of Tolerance condition of DC Calibrator or any reference std General Measurement Device and Calibration Topics 1
C Reasons for Approval Signatures for Records 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 16
V Monitoring Specific Reasons and Categories of Yield Loss of Online Rejects ISO 13485:2016 - Medical Device Quality Management Systems 1
P 25 Reasons why I owe my mother Funny Stuff - Jokes and Humour 0
K Reasons for Issuing Uncontrolled Documents Document Control Systems, Procedures, Forms and Templates 10
S Root Cause Analysis Taxonomy - Categorising the reasons for non-conformances ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
M Top Three Reasons why TPM (Total Productive Maintenance) Initiatives Fail Manufacturing and Related Processes 39
P Seeking sample Resignation Letter - Health and Relocation reasons Career and Occupation Discussions 3
E What are the main reasons to update data in MDS Sheet? RoHS, REACH, ELV, IMDS and Restricted Substances 4
M Practical Reasons Behind The ISO 13485/QSR Regulations ISO 13485:2016 - Medical Device Quality Management Systems 6
T Reasons for retaining Obsolete Documents and Retention Time Document Control Systems, Procedures, Forms and Templates 13
Q Dock Audit - Reasons to do dimensional checks during product dock audit Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
Wes Bucey More reasons to think before clicking on links After Work and Weekend Discussion Topics 12
J Reasons for Implementing ISO 9001 - Findings from a Survey of 326 Businesses The Reading Room 0
N Non UKAS certification bodies - reasons for their avoidance required... Registrars and Notified Bodies 41
Q Top 10 reasons why ASQ is not ISO 9001 registered ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 7
K Compelling reasons for a certifying agency to withdraw a ISO certificate? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
C Reasons for early termination of an audit? General Auditing Discussions 23
A Reasons to Continue QS-9000 in a Company? QS-9000 - American Automotive Manufacturers Standard 4
Sidney Vianna Continual decline of ASQ - can it be saved? Nov 2019 ASQ - American Society for Quality 20
Marc The Continuing Decline of Google Search - 2013 - 2014 Coffee Break and Water Cooler Discussions 37
Wes Bucey Disturbing news - No decline in medical errors World News 11
Marc The Decline: The Geography of a Recession in the US - 2007 thru July 2010 Career and Occupation Discussions 1
M General decline in good manners / common courtesy? Coffee Break and Water Cooler Discussions 26
K Statistical Hypothesis Testing to prove signficant quality improvement or decline Statistical Analysis Tools, Techniques and SPC 6
G ISO 13485 Certification - Can we get the ISO 13485 certification prior to shipment of the device? ISO 13485:2016 - Medical Device Quality Management Systems 6
Richard Regalado Informational ISO/IEC DIS 27001:2021, to be published soon. IEC 27001 - Information Security Management Systems (ISMS) 0
Q Audit report template ISO 9001/14001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
N Does anyone use SGS for ISO 13485 / CE certification Registrars and Notified Bodies 0
Q Process matrix examples of ISO 9001 & 14001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
S Need ISO 15189:2012 Documentation toolkit. Document Control Systems, Procedures, Forms and Templates 0
chris1price Archiving of paper records - ISO 9001 7.5.3.1b Records and Data - Quality, Legal and Other Evidence 4
M Transferring ISO 17025 from one company to another ISO 17025 related Discussions 1
D Common practices in ISO 9001 deployment ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
Q ISO 9001-2015 Internal audit finding Internal Auditing 12
P Audit check for IT company (ISO 9001) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Label Making & Printing Standards ISO / ASTM ISO 13485:2016 - Medical Device Quality Management Systems 5
Sidney Vianna Interesting Discussion Should ISO 9004 be changed from a guidance document to a requirements standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
Ed Panek ISO 13485:2016 Section 5.5.3 ISO 13485:2016 - Medical Device Quality Management Systems 3
Q Do these certificates of calibration meet ISO 9001 requirements for traceability to NIST? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
ebrahim QMS as per ISO 13485, Clause 4.2 Requirements for regulatory purposes for Medical Devices Authorized Representatives. ISO 13485:2016 - Medical Device Quality Management Systems 3
S ISO 2768-mk print call out Other ISO and International Standards and European Regulations 11
T ISO 17024, clauses 4.3.8. and 5.1.1. Other ISO and International Standards and European Regulations 4
C ISO 14001:2015 6.1.3 Compliance Obligations - Legal requirements monitoring ISO 14001:2015 Specific Discussions 0
C Requirement to link Quality Manual to ISO 9001 clause numbers? ISO 13485:2016 - Medical Device Quality Management Systems 13
D ISO 13485 scope (implantable) - Polymers for dental application EU Medical Device Regulations 9
W First time being audited (ISO 9001), asking for advice ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9

Similar threads

Top Bottom