SBS - The best value in QMS software

TickIT vs.ISO 9000-3 vs. ISO 9001 vs. CMM/SEI guidelines @ Level 3

J

J.R. Strickland

#1
Does anyone have any information on ISO 9000-3 and TickIT and the impact on this with the pending release of ISO 9000:2000? Will ISO 9000-3 be updated? My company, currently operating under the CMM/SEI guidelines @ Level 3, is evaluating TickIT registration due to some customer inputs. Our concern is we could get registered this year and have an obsolete certificate by December if ISO 9000-3 is not updated. Any information would be appreciated.
 
Elsmar Forum Sponsor

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#2
I thought I read somewhere that ISO 9000-3 was being phased out. If I remember where I saw that I'll get back with you.
 
A

Andy Bassett

#3
Whilst we are on the subject, i recently turned a job down because it involved building a companies processes around this standard, and i know nothing about it.

Does anyone want to have a go at outlining this standard?. Is it wildly different from 9001/2? What is the key content.? Is it unheard of for Software companies to register to the normal ISO 9001/2

Regards

------------------
Andy B

[This message has been edited by Andy Bassett (edited 12 July 2000).]
 
M

Mike A

#4
A new version of the TickIT Guide is being prepared at the moment for release at the end of the year. The new Guide addresses the requirements of 9000:2000, and also takes into account ISO 12207 - Software life cycle processes.

Hope this helps.
 
A

Andy Bassett

#5
I may have to face this company again soon, is there anybidy out there who could give me for example an brief explanation about the differences between ISO 9001 and ISO 9003.

I would appreciate the help.

Regards


------------------
Andy B
 
#6
A link that may explain how ISO 9000-3 (guidance on implementing ISO 9001 for software), rather than ISO 9003 (Final Inspection and Testing) is given below: ***DEAD LINK REMOVED***
Good Luck
 
M

Mike A

#8
A point that sometimes causes confusion is that, if you are developing a quality system for registration to ISO 9001 and TickIT, the assessors will audit your system against the 20 clauses of ISO 9001 - not against the TickIT Guide or ISO 9000-3.

They will use the Auditor Guidance section of the Guide for interpretation, but your assessment report, non-conformances etc will all be referenced to ISO 9001 (or 9002/9003 if reduced scope).

Until a year ago software producing companies in the UK could only obtain combined ISO 9000/TickIT certification, but this requirement has now been changed, and you can now be registered to ISO 9001 alone.

However, since 9000:2000 incorporates a lot of the process-oriented requirements that are missing from 9000:1994, so the new standard should relate better to IT than the old one did, and companies may choose ISO 9001 rather than ISO 9001/TickIT.

------------------


[This message has been edited by Mike A (edited 09 August 2000).]
 
V

venkat

#10
I would like to know the specific differences between ISO 9000:2000 and TickIT.

Where Can I donwload the copy of tickit guide.
I am aware that it is not available for download at Tickit site.

Apart from that is there any site where I can download
Any help from the viewers please
 
Thread starter Similar threads Forum Replies Date
Hershal Couple of generic TickIT and ISO 27000 questions IEC 27001 - Information Security Management Systems (ISMS) 9
F TickIT vs. ISO9000-3 vs. ISO 9001 - What are the Differences? Software Quality Assurance 7
C TickIT presentation Software Quality Assurance 3
R Latest TickIT Version as of February 2005 - Issue 5 Software Quality Assurance 2
K Different between the ISO9001:2000 and the Tickit standard in software Software Quality Assurance 2
V Tick IT - Regional representative for TICKIT at Chennai Software Quality Assurance 5
N A TickIT strategy Software Quality Assurance 1
R Pointing in the right direction for TickIT - Software Development Processes Software Quality Assurance 2
M Scope for ISO 13485 Certification of a Translation Service Provider ISO 13485:2016 - Medical Device Quality Management Systems 1
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 1
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) 8
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

Similar threads

Top Bottom