ISO 17024 - Personal Certifications Programs Checklist

Elsmar Forum Sponsor
T

The Specialist

#12
Looks good many thanks:)

You are welcome!

Problem with this standard is that (i don't believe) there is a 'standardised' check-list.

You may have to construct one, based upon the points highlighted within the document posted...


Anyone.... Please correct me on this if I am misinformed.
 
#14
Apologies if I have put this in the wrong area of the forum but struggled to find anything on 17024.

Would anyone have a 17024 checklist that I could have, I have checked the attachment list without any luck?

Many thanks,

Chris
Chris:
I was responsible for developing an ISO/IEC 17024 Lead Auditor course a few years ago. What type of audit are you doing? That helps with determining what type of checklist you might need!
 
#16
Hi,

I have attached my starter for 10 as a guide, not formatted or in any sort of order at the moment as to what I am after, does this help?
C
OK, so what's with the title, Chris, 27004? Are you trying to confuse the team here? Do we get bonus points for pointing this out or have you been watching too much University Challenge...:lmao:

So, you turned the standard into a bunch of yes/no type questions...you still need to tell us what this audit is about...:popcorn:
 
C

chris02 - 2011

#17
Sorry about the doc title brain going.:eek:

Based on your answer I think I am obviously missing something here.

What I am trying to do is compile a checklist of all of the requirement of 17024, so that we can check all of the processes / systems we already have in place and then link our findings to actual documentary evidence.

C
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#18
OK, so what's with the title, Chris, 27004? Are you trying to confuse the team here? Do we get bonus points for pointing this out or have you been watching too much University Challenge...:lmao:

So, you turned the standard into a bunch of yes/no type questions...you still need to tell us what this audit is about...:popcorn:
You could be a bit more professional and courteous (if not helpful as well) in your reply.

Sorry about the doc title brain going.:eek:

Based on your answer I think I am obviously missing something here.

What I am trying to do is compile a checklist of all of the requirement of 17024, so that we can check all of the processes / systems we already have in place and then link our findings to actual documentary evidence.

C
I have changed the name of the file you attached.
 
#20
Sorry about the doc title brain going.:eek:

Based on your answer I think I am obviously missing something here.

What I am trying to do is compile a checklist of all of the requirement of 17024, so that we can check all of the processes / systems we already have in place and then link our findings to actual documentary evidence.

C
No problem, Chris - I was trying to inject a little levity here! Not many of the readers would have understood the 'starter for 10' comment! Luckily, being a Brit, I did! Hence the :lmao::lmao: But then again, I suppose not everyone has the same humo(u)r...

Are you doing an audit of an ISO/IEC 17021 based management system? Is this for preparation to be accredited? To give you a helpful reply, I/we need a bit more information about the purpose of creating this checklist, because no-one would want you to go to all that work - retyping the standard in checklist format for it to miss the mark! So maybe you'd tell us a little more about the circumstance you're facing...
 
Thread starter Similar threads Forum Replies Date
T ISO 17024, clauses 4.3.8. and 5.1.1. Other ISO and International Standards and European Regulations 4
Marc ISO 17024 - New accreditation standard - What is it? Is it rational? Do we need this? ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 3
Sidney Vianna RABQSA International - ISO/IEC 17024:2003 ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 10
S Need ISO 15189:2012 Documentation toolkit. Document Control Systems, Procedures, Forms and Templates 0
chris1price Archiving of paper records - ISO 9001 7.5.3.1b Records and Data - Quality, Legal and Other Evidence 4
M Transferring ISO 17025 from one company to another ISO 17025 related Discussions 1
D Common practices in ISO 9001 deployment ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
Q ISO 9001-2015 Internal audit finding Internal Auditing 12
B ISO 17025:2017 risk management Risk Management Principles and Generic Guidelines 0
P Audit check for IT company (ISO 9001) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Label Making & Printing Standards ISO / ASTM ISO 13485:2016 - Medical Device Quality Management Systems 5
Sidney Vianna Interesting Discussion Should ISO 9004 be changed from a guidance standard to a requirements standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
Ed Panek ISO 13485:2016 Section 5.5.3 ISO 13485:2016 - Medical Device Quality Management Systems 3
Q Do these certificates of calibration meet ISO 9001 requirements for traceability to NIST? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
ebrahim QMS as per ISO 13485, Clause 4.2 Requirements for regulatory purposes for Medical Devices Authorized Representatives. ISO 13485:2016 - Medical Device Quality Management Systems 3
S ISO 2768-mk print call out Other ISO and International Standards and European Regulations 11
C ISO 14001:2015 6.1.3 Compliance Obligations - Legal requirements monitoring ISO 14001:2015 Specific Discussions 0
C Requirement to link Quality Manual to ISO 9001 clause numbers? ISO 13485:2016 - Medical Device Quality Management Systems 13
D ISO 13485 scope (implantable) - Polymers for dental application EU Medical Device Regulations 9
W First time being audited (ISO 9001), asking for advice ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
John C. Abnet ISO 26262 ISO 26262 - Road vehicles – Functional safety 3
Marc ISO 26262- Road vehicles – Functional safety ISO 26262 - Road vehicles – Functional safety 0
John C. Abnet ISO 26262 IATF 16949 - Automotive Quality Systems Standard 0
A ISO/DIS 15223-1:2020 - Country of manufacture label (IEC 60417 No. 6049) - Which national law requires this symbol? Other Medical Device Related Standards 0
P ISO 14644 Class 8 Cleanroom Air Filter Requirements Other Medical Device Related Standards 4
K PDCA cycle and ISO processes alternative model Quality Management System (QMS) Manuals 14
N ISO 13485 7.3.9 Change control in medical device software ISO 13485:2016 - Medical Device Quality Management Systems 6
A ISO 13485 procedure change and reflect to legacy manufacture items ISO 13485:2016 - Medical Device Quality Management Systems 2
D ISO 13485 & CE Certification for Surgical Gloves CE Marking (Conformité Européene) / CB Scheme 0
S ISO 11137- Simulated product vs SIP Other Medical Device Related Standards 2
D Which ISO Standard to purchase? ISO 13485:2016 - Medical Device Quality Management Systems 7
V ISO 10360-5: 2020 Gap analysis and Action plan Excel .xls Spreadsheet Templates and Tools 1
Q ISO 9001 - Reseller Exclusions ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
S Inventory Listing and ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 3
C ISO 45001 6.1.2.1 Hazard Identification Occupational Health & Safety Management Standards 1
T The difference between ISO 14644-3:2005 and ISO 14644:2019 Other Medical Device Related Standards 2
S Any ISO standards around Artificial Intelligence and Machine Learning? Medical Information Technology, Medical Software and Health Informatics 4
R AS9100D internal audit checklist or ISO 9001 2015 to AS9100 D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
M ISO 13485:2016 Certification Scope ISO 13485:2016 - Medical Device Quality Management Systems 2
N ISO 9001 - Training business with fewer than 5 employees ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
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
J Opportunity in ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 27
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 17
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

Similar threads

Top Bottom