SBS - The best value in QMS software

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...
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#3
Does anyone here have any experience with IDEF0 / IDEF3?
 

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
D Reports under change management | ISO 13485:2016 & ISO 9001:2015 ISO 13485:2016 - Medical Device Quality Management Systems 3
P ISO 8 classified medical manufacturing room Qualification and Validation (including 21 CFR Part 11) 1
Le Chiffre Online training available for ISO/IEC 17021-1: Requirements for bodies providing audit and certification of management systems Training - Internal, External, Online and Distance Learning 3
B ISO 6508 and portable hardness measurement instruments General Measurement Device and Calibration Topics 0
M Scope for ISO 13485 Certification of a Translation Service Provider ISO 13485:2016 - Medical Device Quality Management Systems 7
S Knee Implant (Femoral -Cobalt chrome)-Sub chronic toxicity test (ISO 10993-11)choice of root Medical Device and FDA Regulations and Standards News 2
Sidney Vianna Release of ISO 10013:2021, Quality management systems – Guidance for documented information Other ISO and International Standards and European Regulations 0
K Integrating ISO 9001:2015 with ISO 17025:2017 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Q ISO 13485 7.5.6 Validation - Off the shelf Software ISO 13485:2016 - Medical Device Quality Management Systems 3
A ISO 13485 Certification for Resin Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 4
R Remote Audits for ISO 9001 (or any other standard) General Auditing Discussions 29
A ISO 13485 Sterilization Clause Applicability ISO 13485:2016 - Medical Device Quality Management Systems 7
K ISO 13485 and compliance of electronic signature ISO 13485:2016 - Medical Device Quality Management Systems 5
T ISO 13485 - Assembly instructions written vs. online ISO 13485:2016 - Medical Device Quality Management Systems 5
M ISO 13485:2016 internal audit checklist Medical Device and FDA Regulations and Standards News 5
D ISO 17021 Certificate Registrars and Notified Bodies 1
X ISO 17025 certification for Laboratory for online gambling products ISO 17025 related Discussions 3
C ISO 19227 Validation Cost Other Medical Device Related Standards 2
N 93/42/EEC certification without ISO 13485 EU Medical Device Regulations 3
T Relationship between ISO 9001 and ISO – IEC BS EN 870079- 34 2020 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
M How Specific in an ISO 13485:2016 Scope for a Contract Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 9
A ISO 13485 for Class 1 Medical Device ISO 13485:2016 - Medical Device Quality Management Systems 7
S Sequence of ISO 9001:2015 Implementation Steps ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
qualprod Business Continuity Planning in ISO 9001? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
T Help with BS EN ISO - IEC 80079-34 2020 (Explosive atmospheres QMS) Other ISO and International Standards and European Regulations 0
C Sampling - ISO 16269-6 vs ISO 2859 Other ISO and International Standards and European Regulations 0
Brizilla Employee Data Privacy Policy - ISO 9001:2015 requirement(s)? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
R ISO 17025 - ISO Guides 33 & 80 ISO 17025 related Discussions 1
0 ISO 13485:2016 Chapter 8 Integration of the subsections ISO 13485:2016 - Medical Device Quality Management Systems 3
S ISO 9001:2015 Internal Auditing Internal Auditing 8
Q Process: Knowledge Section 7.1.6 of ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
N ISO 27001 for Jumb Burger - Risk Assessment sheet IEC 27001 - Information Security Management Systems (ISMS) 10
H What ISO certification is for an IT department? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
M Change in Constitution / Ownership of firm -------ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 1
P ISO 9001 certification with zero customers? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
M ISO 14971 Determination of Competent Persons ISO 14971 - Medical Device Risk Management 4
R Clinical accuracy and repeatability of IR(infrared) thermometer, no maximum error criteria is recommended in ISO Other Medical Device Related Standards 11
Q The scope of ISO 21534 Other Medical Device Related Standards 0
A What must be recorded? (ISO 9001:2015, subclause 10.2) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
M ISO 14971:2019: Criteria for overall residual risk ISO 14971 - Medical Device Risk Management 4
B Updated IATF 16949 - Will IATF 16949 get revised when ISO 9001:202X is released? IATF 16949 - Automotive Quality Systems Standard 4
S ISO 9001:2015 vs 21 CFR Part 211 matrix Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
N Quality Compliance Officer - ISO 13485, London Job Openings, Consulting and Employment Opportunities 1
T ISO 17025: Lockout/Tagout Requirement ISO 17025 related Discussions 1
S ISO 9001 implementation in a Gold exporting business ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
M Does the ISO 9001:2015 standard require a disaster recovery plan or emergency response plan ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
E ISO 13485 QMS certification as a Supplier ISO 13485:2016 - Medical Device Quality Management Systems 8
A Environmental Compliance obligations and risks (ISO 14001:2015 6.1.3) ISO 14001:2015 Specific Discussions 3
R ISO 17025 vertical audit checklist wanted Document Control Systems, Procedures, Forms and Templates 2

Similar threads

Top Bottom