SBS - The best value in QMS software

Should the billing process be part of ISO 9001:2008?

Should the billing/invoicing process be explicitly part of ISO 9001:2008?

  • Yes. Billing/invoicing processes should be explicitly part of the new ISO 9001

    Votes: 24 55.8%
  • No. Billing/invoicing processes should not be part of the new ISO 9001

    Votes: 19 44.2%

  • Total voters
    43
G

Greg B

#41
I see that a lot of people agree with me that it should not be included but I would like to point out to those that say their current financial audits are just checking the dots on the i's and crosses on the t's are really simplifying the process (at least here in Aust). Financial audits have taken on a greater role and now audit the process. Our last audit identified that we carried far too much stock (Product and Spare), that our Stock taking techniques were inadequate and could cause 'double ups' in accounting and followed invoices from product to customer. They have been doing this for several years now and I can attest to a greater tolerance for them now than when everyone thought they just sat around counting pennies. I will not have the system then be audited or answer to ISO. the same as i don't let Environment or Safety fall under our umbrella also. When the world issues an all encompassing BUSINESS Standard that deals with whole of business (including maintenance) I will allow finance to fall within my realm. Push a better business appreciation rather than adding extra work for me.
 
Elsmar Forum Sponsor
J

Joe Cruse

#42
I agree with your post wholeheartedly, Greg. :applause:

We had a similar experience with accounting and our external accounting auditing. This past cycle, especially, is helping us look at some business practices, and make improvements for the business (that will be showing up in the CI index of our QMS).

I also see no need for our QMS to include this area, when it is already being covered quite well in another way.
 
J

JadeS

#43
We identified all Accounting functions, including billing/invoicing as support processes when mapping the processes. To not include them would have left an open loop. They are also identified throughout the 'Customer Oriented Processes'.

Jade
 
R

Rick St

#44
We have decided to assess what we call "administrative quality." This would include pricing errors, order entry errors, etc. These are then worked the same way we work product quality issues. Administrative quality isn't defined by our QMS, but we think it falls under the customer satisfaction element of the standard.
 
D

Denis9001 - 2007

#45
Billing is part of the business process and a common source of customer dissatification. So, if the standard is not to have any process gaps it should include billing. But it must be clear that it is not a financial audit. We don't care about the company accounts, just that the customer is billed correctly. Perhaps the customer-related processes section could be modified to cover this. After all the bill is in many cases what the law considers (I think) to be the "contract" between supplier and customer.

Really the standard should cover all business functions. That it doesn't directly handle areas like production equipment baffles me. But that's for another thread.

If a customer was overbilled and paid or the credit terms were wrong or invoices sent out late, the customer may be unhappy but would the financial auditor care or cover this. My ISP recently cut off my connection without payment reminder or disconnetion notice because 1 dollar was outstanding on a monthly bill from 3 months ago. I was hopping mad and if I find they made a mistake will give them another earbashing on the phone,
 
Last edited by a moderator:
M

Madfox

#46
Yes, and no...
...and "billing" goes both ways, getting paid and paying suppliers.

I don't believe in getting into the nitty-gritty financials, however management should be aware of:
a) billing (inbound/outbound) issues
b) billing performance (most are keenly aware of avg. outstanding A/R, but few regarding avg. outstanding A/P)

A close friend (with an NYSE-listed org) lost a HUGE account simply because their client's CFO got fed up with trying to get a correct bill.

When I'm asked about "process engineering" here's my example (true story, been to the company, know the salesperson):
A printing company had a client who had been with them for over 12 years. The client had started as a two-person company and now accounted for approx. 8% of the printer's revenue, and about 12% of the account manager's annual income (commission-based).

The client's founder/president still maintained the "up close and personal" relationship with the printer, literally paying the bills with his own business credit card. Well, he gets a call from someone in A/R who, very coldly, simply states "We're not accepting credit cards anymore, we will be sending you a credit reference form to establish a line of credit....blah, blah, blah."

What irked the client was being treated so rudely, and he wrote the printer's president notifying them that their relationship was over. The client's account manager and the sales manager had no idea the accounting dept. was implementing this change regarding credit card usage. The sales person had to be peeled off the ceiling!

A silo-oriented organization: "Congratulations to our accounting dept. for decreasing costs incurred from credit card transactions!" "Hey sales, what's your problem, your numbers are way off!"
Would this have happened in a process-oriented organization?
 

Sidney Vianna

Post Responsibly
Staff member
Admin
#47
A silo-oriented organization: "Congratulations to our accounting dept. for decreasing costs incurred from credit card transactions!" "Hey sales, what's your problem, your numbers are way off!"
Excellent example. :agree1:

Would this have happened in a process-oriented organization?
I don't know, but obviously not in a customer-centric organization. Hey, gotta use new buzzwords...
 
R

Rik Arkell - 2008

#48
Couldn't agree more. 'Finance' audit only covers the accuracy/fraud etc. They are not interested in whatthe customer thinks, only that everything 'stacks up' from a fiscal point of view. ISO looks further at issues affecting the customer - e.g. timliness of invoicing, accuracy and so on.

There is also the other softer issue - in omitting staff involved in invoicing what message are you delivering to them regarding qualitiy in their work?
Cheers,
Rik

Cheers,
Rik
 
S

shawnann

#49
NO they shouldn't be apart of the ISO requirements.

1. Financial information for companies are private information.
2. The billing and receipt of payments has nothing to do with the quality of the work being performed by your company, in the matter of product.
3. There is no reason for an outside company to audit your financials of the business.
4. What next, auditing the employees for time off, sick days, etc.?
 

Sidney Vianna

Post Responsibly
Staff member
Admin
#50
NO they shouldn't be apart of the ISO requirements.
I think you mean a part
2. The billing and receipt of payments has nothing to do with the quality of the work being performed by your company, in the matter of product.
Your definition of quality is too narrow and inconsistent with the ISO 9000:2005 definition. Do you disagree that erroneous billing is one of the most common sources of customer dissatisfaction?
 
Thread starter Similar threads Forum Replies Date
A Should we assign the PRRC before the date of application of MDR (26 May 2021)? EU Medical Device Regulations 0
J UDI-DI how should we interpret Device version or model to determine if a new UDI-DI is needed? EU Medical Device Regulations 0
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
A Should I take an online course for a career in Occupational Health and Safety? Career and Occupation Discussions 2
J Should a Class 1 medical device with an option to measure body weight be considered Class 1m? EU Medical Device Regulations 0
K Should APQP/PPAP has its own section in a QM? Quality Management System (QMS) Manuals 1
S What should i choose for "testing procedure" characteristics? (N95) General Information Resources 0
P Should eIFU link per ISO 15223-1:2016 be added to labels out of scope of Reg 207/2012? EU Medical Device Regulations 1
S Which Sampling Plan(s) Should I Use? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
A Document release vs its related training. Which should come first? ISO 13485:2016 - Medical Device Quality Management Systems 18
S Which department should prepare the control plan? could you show me a standard regarding to this matter. FMEA and Control Plans 17
J Help settle a disagreement: Should external providers of preventive maintenance be on your ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
N Master Samples - What should we be keeping? IATF 16949 - Automotive Quality Systems Standard 9
G Supplier delivered recent PPAP, should he deliver yearly layout inspection? IATF 16949 - Automotive Quality Systems Standard 4
John Broomfield Vote - Should ISO9004 Become a Requirements Standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
A Capability Study - in the beginning of your career what should you have known about the tool Quality Tools, Improvement and Analysis 11
J Should Loading and Unloading be Included in Cycle Times? Lean in Manufacturing and Service Industries 14
E Manufacturers should develop a testing device for covid19 Service Industry Specific Topics 0
T 510(k) submission - Which name should I use in the submission? Other US Medical Device Regulations 3
N ISO 19011:2018 - 5.4.2 "...audit program should engage in appropriate continual development..." Training - Internal, External, Online and Distance Learning 4
G Should I perform Gage R&R only at the beginning of a new project? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 6
DuncanGibbons Should the requirements FAA/EASA Part 21 be addressed within the QMS and AS9100D quality manual? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
M Should 510(k) Predicates be Actively Listed Devices? Other US Medical Device Regulations 12
B Why the Greek god Hephaestus should have done a design FMEA (DFMEA) on his giant robot APQP and PPAP 1
J On PFMEA for danger labels - Label always should be assigned severity 10 ? FMEA and Control Plans 3
H Who should be listed as the manufacturer/distributor on the box? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 15
M MDR, RED and LVD - Should our device comply with them? EU Medical Device Regulations 3
BeaBea How Many Processes should be created for each Department? Process Maps, Process Mapping and Turtle Diagrams 5
M Should volume of sales be factored into risk probability assessments? ISO 14971 - Medical Device Risk Management 33
MrTetris Should potential bugs be considered in software risk analysis? ISO 14971 - Medical Device Risk Management 5
S Should safety checks be included in the Control Plan? IATF 16949 - Automotive Quality Systems Standard 5
M Which incubation condition should be selected to recover both bacteria and fungus effectively Miscellaneous Environmental Standards and EMS Related Discussions 3
D Is there a specific location for PPE such as safety glass holders and glove dispensers should be mounted Occupational Health & Safety Management Standards 10
Robert Stanley Which Registrar Should I Choose for ISO 9001:2015 registration? Registrars and Notified Bodies 10
M Who should receive the bills from suppliers and vendors, account payable or procurement? Consultants and Consulting 4
V IATF 16949 8.4.1 Control of externally provided processes, products and services - Should the CB be on our Approved Supplier List? IATF 16949 - Automotive Quality Systems Standard 10
A We are ISO 13485:2016 should we be audited to ISO 14971 ISO 13485:2016 - Medical Device Quality Management Systems 16
E Received a Major finding during IATF Surveillance audit for loss of BIQS Level 3 (more than 6 SPPS in 6 months)...how should we address SYSTEMIC CA? IATF 16949 - Automotive Quality Systems Standard 11
J Organization merger. Should we keep two separate ISO 13485 certificates? ISO 13485:2016 - Medical Device Quality Management Systems 6
S Companies that maintain your machine should be in ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
S Use of "Shall" versus "Should" in Procedures ISO 13485:2016 - Medical Device Quality Management Systems 26
D Class II medical device - When should a complaint be closed? Customer Complaints 6
Sidney Vianna IATF 16949 News Presentations from the latest IATF Stakeholder Event - Expectation that IATF 16949 certification should equate with product quality. Misguided? IATF 16949 - Automotive Quality Systems Standard 7
L Clause 0.4 of ISO 9001 and EHS - Where should I stop the inclusion of EHS in my QMS ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
Ed Panek Part 11 Self Certify Memo - What else should it cover? Qualification and Validation (including 21 CFR Part 11) 5
H Should I mention machine/Equipment password In SOP? Qualification and Validation (including 21 CFR Part 11) 4
D How long should we keep the spare parts available for our medical device, after we have stopped the production? ISO 13485:2016 - Medical Device Quality Management Systems 0
H Statistical Techniques Procedure - What should be included Document Control Systems, Procedures, Forms and Templates 4
Q How should I analyze measurement correlation between me and customer? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 12
Sidney Vianna Interesting Discussion ISO 9001:2024 - What should be changed in the next Edition of ISO 9001? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 114

Similar threads

Top Bottom