Practically implementing ISO 9001:2000 Clause 7.2.2 Contract Review

N

Nikki Wessner

#1
We are an ISO 9001:2000 certified company and have been for 7 years. We receive 80% of our orders via a faxed PO from our customers. The majority of these have incorrect pricing noted. This is due to a variety of reasons. To name a few: Customers have not updated their systems to reflect our recent price increase, Customers receive a volume discount on a previous order and assume that the pricing will be the same no matter what the quantity or NO price is given.

If there is a large discrepancy between the customer's given price and our system generated price, then we halt the order process and communicate with the customer to get resolution. However, if the price is only off by a couple dollars then we will typically place the order and fax them back an order confirmation clearly advising them to "note correct pricing". To stop the process for every order would require a large increase in resources on our part, and also cause problems with delivering product on time. Management feels that to do this would increase customer complaints and make it difficult to do buisness with our company.

As lead internal auditor, I am unsure how to move forward. In 7.2.2, it clearly states that contract review should occur "prior to the organization's commitment to supply a product to the customer"...Which we are "technically" not doing, since we place the order (for small price discrepancies) without getting prior agreement from the customer on this price. To what extent does this apply? Does this include small price discrepancies?

ANY advise would be helpful here. IF we are noncompliant, is there information out there on how other certified companies handle this dilemna?

Thanks!
Nikki
 
Elsmar Forum Sponsor

Jen Kirley

Quality and Auditing Expert
Leader
Admin
#2
Re: Practically implementing ISO 9001:2000 7.2.2

Welcome to The Cove Nikki! :bigwave:

When I think of contract review I think of things like customer requirements, special handling needs, specifications used, and so on.

I don't normally think of prices as ISO 9000 goes. Seems odd, doesn't it? No doubt there are vast crowds of people with problems like yours. But unless price is a defined quality aspect I wouldn't consider it a hanging offense.

Maybe I'm walking on thin ice here, but I'd consider including a contractural clause permitting the type of events you described. Pricing flexible within 10% or else prior notification, for example.

IMHO, what matters in contractural review is what the customer says matters in the decision to buy: what constitutes goodness of quality and/or service.

That said, how often do you change prices? Would it help to install an internet based ordering method in which you could keep the prices current for them? If it's possible to help out the relationship by cleaning this up, you could be saving your folks some valuable time while complying with 7.2.3, 8.2.1 and 8.5.1.
 
N

Nikki Wessner

#3
Re: Practically implementing ISO 9001:2000 7.2.2

Interesting...our customer service manager brought up the question "Does this review apply to pricing..." We assumed it did because we were considering everything on the PO a requirement.

I appreciate your input.
 

Jen Kirley

Quality and Auditing Expert
Leader
Admin
#4
Some people would indeed consider everything on a PO as a requirement. I would consider that an audit pot hole if my prices changed often enough to resemble falling out of requirements.

Some POs include a clause saying something like "Prices subject to change". If that bothers your customers, it should be negotiated before the order is finalized. If your customers don't care, the pricing issue could seem more important internally than externally.

Seems to me the cleanest method is to automate the ordering process so the price is placed up front.
 
N

Nikki Wessner

#5
Thanks for your time Jennifer!

Our prices change annually, or they have the last couple of years. I'm not sure what you mean by "automating the ordering process"...we have a web shop, but it isn't widely used (about 7% of orders come in from this source). Most of our orders are faxed to us...either from a hand written PO or one generated from the customers ERP system. I'm having trouble understanding how this could be automated to state a price upfront.

Could you point me in the direction of any white papers or articles written regarding this?

Again, thank you for your insight! :thanks:
 
G

Greg B

#6
We receive most of our orders the same way (fax or email) but they are first vetted by the Marketing Department for approval. We raise a Sales Order Confirmation (SOC). Marketing approve price/sale/Specs etc and then send the SOC on to production. TProduction sign it to say they can make it by the due date with the specs required. It is THEN approved and not before. So it is a simple two step process.
Marketing yes/no
Production yes/No

If either party does not approve the order a secondary process is implemented to inform the customer but it is all recorded on the original SOC. It is an easy system...well, at least in our company. We have a Product Release form at the end of the order and the SOC is the master to approve the order and place it in the system.
 
Last edited by a moderator:
N

Nikki Wessner

#7
Hi Greg!

Are your orders for custom pieces or services? The reason I ask is that we sell an "off-the shelf" product. Orders come in at a rate of approximately 10000 a month (about 5000 of that is fax/email). What I'm concerned about is the feasibility of confirming each order before it is entered. I believe a simple process can be built (and I appreciate you sharing your process); however, the added resources in order to implement such a process would be huge.

Thanks,
Nikki
 
C

CliffK

#8
I would claim that your company doesn't have to change much, if anything.

ISO 9001 7.2.2 says that you must review requirements before you commit to supply a product.

When does that commitment occur? For orders that unexpectedly arrive by fax, your company doesn't commit until you send out the confirmation.

Now, if the customer has requested a quote and you've provided one, you're bound by the terms of the quote as soon as the customer's PO arrives.

Which brings us to the one thing you might want to fix. Are your company's quotes clear about time limits or quantity limits? Is there language in the quotes that might lead customers to believe that a one-time quantity discount applies to all future business? If so, that situation would be worth addressing.

But if your order entry system works otherwise, don't change it because of ISO 9001. You don't need to.
 
N

Nikki Wessner

#9
:thanx:

Your response has helped me understand the standard a bit more and how to defend our decision (if by chance this comes up in our next external audit).

I think we could do a better job in communicating the terms of volume discounts and pricing on our Sales Order Acknowledgment. This is a doable task :)

Thanks!!

Nikki
 
G

Greg B

#10
Hi Greg!

Are your orders for custom pieces or services? The reason I ask is that we sell an "off-the shelf" product. Orders come in at a rate of approximately 10000 a month (about 5000 of that is fax/email). What I'm concerned about is the feasibility of confirming each order before it is entered. I believe a simple process can be built (and I appreciate you sharing your process); however, the added resources in order to implement such a process would be huge.

Thanks,
Nikki
Nikki,

We are a bulk commodities company selling in tonnages ranging from a few tons to thousands of tons, of bulk product. Our system, currently, is a PUSH system but we are changing to a PULL system. This means as the orders come in, the product is planned and produced to meet that order rather than making it and then trying to sell it. We have approximately 100 orders per month and a staff of 4 in marketing, 2 in customer services and then the heads of each production area. I don't know how you would adopt a system for off the shelf items other than as product comes on line it is assigned a product number, entered into a spreadsheet (SS) or database (DB) and then as the orders come in they are married to a final product in the SS or DB. The result would be that each order is handled once and married to a particular product. You could not double up.
When building the SS or DB an up to date pricing schedule should be used and a report automatically generated whenever the customer price does not match the company price. We have a similar system built into our bulk sales. Our marketing people keep our pricing schedule up to date for each customer on a regular basis. if there are any problems after that the customer and marketing discuss it.
 
Thread starter Similar threads Forum Replies Date
D How to practically-conduct, post production phase ISO 13485:2016 - Medical Device Quality Management Systems 1
E How to practically organize the 'Vigilance' function? ISO 13485:2016 - Medical Device Quality Management Systems 7
H Implementing ISO14001:2015 ISO 14001:2015 Specific Discussions 4
A Small Company Implementing ISO 13485 Timeline/Process/Steps Advice ISO 13485:2016 - Medical Device Quality Management Systems 5
E Theoretical project: Implementing ISO 13485:2016 into a start up acrylic bone cement manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 4
G ISO 9001 - when implementing customer requirement ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
K Is implementing Electronic Signatures a Significant Change to the QMS? ISO 13485:2016 - Medical Device Quality Management Systems 10
Moncia Implementing ISO 50001 Sustainability, Green Initiatives and Ecology 21
H Implementing ISO22301 on a Limited Scope Business Continuity & Resiliency Planning (BCRP) 2
J Implementing an ISO 13485 QMS Software ISO 13485:2016 - Medical Device Quality Management Systems 11
Sravan Manchikanti How to interpret '8.3 Control of nonconforming product' for SaMD device while implementing ISO 13485 & MDSAP ISO 13485:2016 - Medical Device Quality Management Systems 7
L Implementing the PRRC role in a company EU Medical Device Regulations 8
A Implementing ISO 20000-1 - Where to start Other ISO and International Standards and European Regulations 4
B Lessons Learned Implementing ISO 50001 (Chemical Engineering Progress) Other ISO and International Standards and European Regulations 0
C How medical device manufacturers are implementing standards like GDPR and HIPAA Other ISO and International Standards and European Regulations 5
M Informational EU – Commission Implementing Decision (EU) as regards the designation of expert panels in the field of medical devices Medical Device and FDA Regulations and Standards News 0
R Implementing Design History Documents/ Technical Documents in the QMS ISO 13485:2016 - Medical Device Quality Management Systems 3
tnorton Lessons learned from implementing Customer Complaints Customer Complaints 1
M Informational Update – MDR and IVDR implementing measures rolling plan – 2 more NBs designated under the new regulations Medical Device and FDA Regulations and Standards News 0
S Implementing a 45001 Health & Safety standard - Internal audit plan wanted Internal Auditing 1
M Informational Commission Implementing Decision (EU) 2019/939 of 6 June 2019 designating issuing entities designated to operate a system for the assignment of Unique Medical Device and FDA Regulations and Standards News 0
J Implementing Machine Replacement Part Reverse engineering technology Manufacturing and Related Processes 4
Q Does anyone have experience implementing a QMS without ISO certification? Quality Manager and Management Related Issues 2
M Informational EU – April 2019 update of the MDR and IVDR implementing measures rolling plan Medical Device and FDA Regulations and Standards News 0
I First Time Implementing Document Control for ISO-9001 - how far back do you go? Document Control Systems, Procedures, Forms and Templates 15
M Medical Device News Last update of the MDR and IVDR implementing measures rolling plan – December 2018 Medical Device and FDA Regulations and Standards News 0
J Implementing EN 62304:2006 on existing and proven medical devices IEC 62304 - Medical Device Software Life Cycle Processes 6
M Medical Device News MDR and IVDR implementing measures rolling plan EU Medical Device Regulations 0
B Implementing an Escalation Process and Andon system Supplier Quality Assurance and other Supplier Issues 1
K EQMS question - Implementing an electronic QMS to support ISO 13485:2016 Quality Assurance and Compliance Software Tools and Solutions 4
T Is there any requirement to be compliant with IEC 62304 while implementing ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 5
armani Compliance Obligations - Implementing 6.1.1 and 6.1.3 NOTE - Determine risks and... ISO 14001:2015 Specific Discussions 1
G Heavy Civil Construction Company Implementing ISO 9001:2015 for Certification ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
K Implementing ISO13485:2016 in the Middle of a New Device Project ISO 13485:2016 - Medical Device Quality Management Systems 1
D Implementing 5S for Multiple Shop Floor Layout Workstations Lean in Manufacturing and Service Industries 2
N FDA Guidelines for implementing Continuous Improvement Process US Food and Drug Administration (FDA) 5
Q Easy Way of "Implementing" Risk in ISO 9001 2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
N Implementing ISO 17025 in a Calibration Laboratory ISO 17025 related Discussions 8
E Does anyone have experience implementing a Tiered QMS? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
A Implementing an AS9100 Aerospace Quality System AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 9
L Implementing ISO 9001 in small Trading Company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
C Implementing a set of bore gages at a machine Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
A Implementing Risk Management in a Medical Device "Distributor Only" company ISO 13485:2016 - Medical Device Quality Management Systems 6
T Implementing a Suspect Counterfeit Identification Program Quality Manager and Management Related Issues 3
O Implementing Lean Intranet Sharepoint Lean in Manufacturing and Service Industries 6
F Implementing ISO 9001:2008 in a new Food Processing company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
J ISO 22301 - Implementing a Business Continuity Management System Business Continuity & Resiliency Planning (BCRP) 15
M Does anyone here have experience implementing PCI DSS (Data Security Standard) IEC 27001 - Information Security Management Systems (ISMS) 10
L Implementing a new quality management system for a new engineering company ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
M Implementing ISO 9001 in an Assembly Plant ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10

Similar threads

Top Bottom