IDEF0 / IDEF3 as ISO 9001:2000 documentation? Implementation of IDEF0 or IDEF3

J

Jean-Philippe

#1
Hi,

As a member of the quality team in a military (NATO) software maintenance/development organization, I was asked to look at the different options to make our quality system (ISO 9001 based) more "process oriented" and to extend its description to "non-core" (support) processes.

I was very much seduced by the tandem IDEF0/IDEF3 approach see A structured approach to enterprise modeling and analysis Could anybody give me practical information on the implementation of IDEF0 or IDEF3 in his/her organization ?
I'd be also very much interested in a real life example of IDEF0/IDEF3 charts (preferably in a software organization).
Finally, has anybody tried to actually use (adapt) the IDEF0-3 documentation set as (base for) a quality manual ?

I know I'm asking a lot, but thanks in advance.

Jean-Philippe Hubin
 
Elsmar Forum Sponsor
A

Al Dyer

#2
I took a quick look through the web site and it looks like a powerfull set of features. I can't help you but maybe we can find someone in the forum.

Any takers!

ASD...
 

DuncanGibbons

Involved In Discussions
#4
I realize this is a very old post. But does anyone have experience using IDEF0 and 3 for development and documentation of processes as part of a QMS? And is it recommended ahead of traditional process flow diagrams?

My two cents, it has better functionality than traditional process flow diagrams and can easily be converted into UML for simulations, although does have a bit of a steeper learning curve.
 
Thread starter Similar threads Forum Replies Date
J ISO 9001 and IDEF0/3 - Military (NATO) software maintenance/development organization Other ISO and International Standards and European Regulations 4
K Applicable ISO 9001 clauses for Human Resources? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
C Clinical Trial using Prototype devices (EU MDR & ISO 14155) EU Medical Device Regulations 3
I IEC 60812 or ISO 14971 for PFMEA? What should we use? ISO 14971 - Medical Device Risk Management 3
I ISO 9000 Where to Start ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 44
M ISO 13485 consultants and auditors with design oriented focus ISO 13485:2016 - Medical Device Quality Management Systems 6
D ISO 9001:2015 Internal Audit Check Sheet ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
H Does ISO state in anyway that we MUST keep physical first piece parts? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
B ISO cl. 5.3 - Ensuring that the integrity of the QMS is maintained ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
A ISO 9001- any advise please with transitioning from a paper based system to eQMS and multi site scope ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
L ISO 20417 crucial changes Other Medical Device Related Standards 1
R ISO 27001 Mandatory Policies , Procedures and Records IEC 27001 - Information Security Management Systems (ISMS) 0
R Use of historical version of ISO standards CE Marking (Conformité Européene) / CB Scheme 3
I QMS and ISO 9001 Misc. Quality Assurance and Business Systems Related Topics 11
E ISO 17025 Key Performance Indicators (KPIs) ISO 17025 related Discussions 5
A ISO 9001:2015 8.5.6 and 7.5.3 Document Control Questions ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
J ISO 9001:2015 Clause 8.2.3 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
LabCat Internal SOP for a validated (ISO) method? ISO 17025 related Discussions 2
L Confusion about ISO 14644 Other Medical Device Related Standards 2
GStough Audit Nonconformances (?) for Suppliers Not Registered to ISO and No Supplier Quality Agreement Exists General Auditing Discussions 24
S Brexit ISO 13485:2016 + Corrigendum - What does a UKCA DoC require? EU Medical Device Regulations 2
M Is complete testing required as per ISO 10993 for materials used in orthopedic implants or is literature review route possible Other Medical Device Related Standards 3
Aliken Recommendation for the ISO 13485 certification company ISO 13485:2016 - Medical Device Quality Management Systems 7
ISO-tired ISO 13485: file structure overview ISO 13485:2016 - Medical Device Quality Management Systems 11
J ISO 10993-1:2018 Format to Perform Risk Management Process US Food and Drug Administration (FDA) 1
B ISO 9001:2015 Registered Companies ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
C ISO Cert and Parent Company is not Certified ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
B Is 14971 Annex C checklist now in ISO/TR 24971 required to complete prior to 510k filing? ISO 14971 - Medical Device Risk Management 3
Q ISO Training Providers to fix careless workers? Training - Internal, External, Online and Distance Learning 19
M PROBLEM IN SCOPE OF ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 6
S ISO 13485 signing of Procedures etc. ISO 13485:2016 - Medical Device Quality Management Systems 10
N ISO 13485 Scope Reduction Other ISO and International Standards and European Regulations 2
Sidney Vianna ISO 37301 - Compliance management systems – Requirements with guidance for use Other ISO and International Standards and European Regulations 2
S ISO 3497 Metallic Coatings Other ISO and International Standards and European Regulations 1
R Basic Lab Practices - related to ISO 17025 testing labs ISO 17025 related Discussions 1
JDJohnson Micrometer & Caliper Calibration (ISO-9001) General Measurement Device and Calibration Topics 26
M Can veterinary implants be ISO 13485 certified? ISO 13485:2016 - Medical Device Quality Management Systems 23
D Audit Report details when ISO 13485:2016 and cGMP 21 CFR 820 are applicable ISO 13485:2016 - Medical Device Quality Management Systems 6
G Why do you guys think ISO 9001 doesn't ask specifically for preventive maintenance? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 29
D Training for ISO 17025 ISO 17025 related Discussions 2
R Looking for ISO 13485 Internal Audit Checklist ISO 13485:2016 - Medical Device Quality Management Systems 8
FuzzyD ISO 13485 change in process ISO 13485:2016 - Medical Device Quality Management Systems 3
D ISO 9001:2015 Calibration Procedures Manufacturing and Related Processes 16
R Interesting Discussion Chapter 7.5 of ISO 13485 for manufacturers of mobile medical applications ISO 13485:2016 - Medical Device Quality Management Systems 4
J ISO Certificate Expiration ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
V ADDING NEW MEDICAL DEVICE / Product, WHEATHER THIS AFFECTS EXISTING ISO 13485 CERTIFICATION? ISO 13485:2016 - Medical Device Quality Management Systems 4
G Auditing Top management: 6.3 ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
S Question regarding AQL - ISO 3951 Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
Sidney Vianna Informational ISO/NP TS 17012 - Guidelines for use of remote methods in conducting audits of management systems Other ISO and International Standards and European Regulations 0
G IT being audited during ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7

Similar threads

Top Bottom