Does anybody have an audit check list for ISO/IEC 17025 to replace ISO/IEC Guide 25

A

Aaron B.

#1
Does anybody have an audit check list for ISO/IEC 17025 to replace ISO/IEC Guide 25 For Calibration Labs. Or how we can obtain it.
 
Elsmar Forum Sponsor
P

pdboilermaker

#3
I have a copy of the 17025 but not a checklist, I am in the midst of a 16949 certification audit for the rest of the week, I would gladly ask my registrar for a checklist for you guys
 
P

pdboilermaker

#5
They have a draft copy of the 16949 audit with a lame question like "is the lab or subcontracted labs iso 17025"
It isnt really what you wanted but let me know if your interested anyway
[email protected]
 
W

walid9610

#6
copy of ISO 17025

dear Mr. pdboilermaker,

i need a copy of ISO 17025 as soon as possible and please provide me the Audit checklist for ISO/IEC 17025.

thanks,

Walid9610

pdboilermaker said:
I have a copy of the 17025 but not a checklist, I am in the midst of a 16949 certification audit for the rest of the week, I would gladly ask my registrar for a checklist for you guys
 

Hershal

Metrologist-Auditor
Staff member
Super Moderator
#7
Often, the accrediting bodies have such checklists available, although you may have to send an e-mail request. The availability of the checklists is normal in North America, and I suspect in other areas of the world also.

Does Lebanon have an accrediting body? If no, then may I suggest some collaboration with Egypt, as they are developing an accrediting body, and may be in a better position to assist your accreditation needs.

Hope this helps.

Hershal
 

Manoj Mathur

Quite Involved in Discussions
#8
Checklist for ISO 17025

I wish I can attach the checklist for auditing this standard. But as you all know I have limitation to attach a file. Hence I am sending this file to Mr. Marc with a request to attach on board.
 
Thread starter Similar threads Forum Replies Date
M Does Anybody have an ISO 22000 internal audit checklist for sharing? Internal Auditing 11
J Does anybody have an audit checklist focused on Manufacturing processes? Manufacturing and Related Processes 8
B Does anybody know how to get older versions of Minitab to work in Windows 10? Quality Tools, Improvement and Analysis 9
I Does anybody use Detection in medical device Design FMEA? ISO 14971 - Medical Device Risk Management 18
L Does anybody have quiz's available? ISO 13485:2016 Training Material Training - Internal, External, Online and Distance Learning 2
A Does anybody know in which Standard can this attached Alarm Symbol be found? Other Medical Device Related Standards 3
A Does Anybody use APIS (IQ-FMEA) Software in this forum? FMEA and Control Plans 2
Y Does anybody have any knowledge in Statistical Bin Limit (SBL)? Statistical Analysis Tools, Techniques and SPC 2
T Does anybody know about EN45014? (Replaced by ISO/IEC 17050-1) Other Medical Device Related Standards 1
Stijloor Does anybody get a job from listings in the Cove? Career and Occupation Discussions 18
W Preventive 5S - Does anybody have any idea about Preventive 5S? Preventive Action and Continuous Improvement 1
M When is a system not a single device? Does anybody know of a guidance document? ISO 13485:2016 - Medical Device Quality Management Systems 11
A IC: 5.15 vs 6.00 sigma - Does anybody here use 5.15 sigma for MSA calculations? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 3
R Iso/tc69/sc4/wg6n48 - Does anybody here know captioned standard? Statistical Analysis Tools, Techniques and SPC 3
J Does anybody can give a help about GR&R Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 3
J Does anybody can give me a help about the calcuation about no defect on 6 sigma level Six Sigma 3
S Does anybody have any idea about EAQF94 standards? IATF 16949 - Automotive Quality Systems Standard 2
W FPS (Ford production system) - Does anybody have any interesting comments? Customer and Company Specific Requirements 8
N Blueprint reading training - Does anybody have any recommendations? Training - Internal, External, Online and Distance Learning 6
A Does anybody have any information about the Firestone tire problem? Nonconformance and Corrective Action 18
M Does 4.5 - Alternative RISK CONTROL apply to the Particular Standards? IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
E Does IVD need to integrate with hospital IT infrastructure? Medical Information Technology, Medical Software and Health Informatics 0
D What does a level 1 (PSW) PPAP actually promise? APQP and PPAP 8
R GS1 DataMatrix code does not meet GS1 Specification EU Medical Device Regulations 0
M Does the scope of ISO 9001:2015 applies to tenders, pricing and sales department of a medical devices distributor? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
K Why does load cell supplier requires force verification General Measurement Device and Calibration Topics 3
M Does C=0 strictly mean 1 bad, all bad, all the time? ISO 13485:2016 - Medical Device Quality Management Systems 6
C Does a medical device active (zinc oxide) needs BPR registration in EU? Other ISO and International Standards and European Regulations 1
D Does Risk Management apply to re-labeler (MDR) EU Medical Device Regulations 1
Ed Panek Does this FDA Requirement Apply to international (not USA) distributors for USA based manufacturing companies? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
S Does anyone have a checklist to prepare for ISO 13485, Stage I audit? ISO 13485:2016 - Medical Device Quality Management Systems 1
S Does a refurbished product required a new UDI? US Food and Drug Administration (FDA) 3
D Change to labelling - does it require a new 510(k)? US Food and Drug Administration (FDA) 5
M What does "constantly" mean ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
N Does anyone use SGS for ISO 13485 / CE certification Registrars and Notified Bodies 0
G Does FDA allows remote approvals of quality documentation. Is there any specific guidance on signing any quality records remotely? Document Control Systems, Procedures, Forms and Templates 1
B Does FDA Registration QSR need to cover non-medical devices for contract repackager? US Food and Drug Administration (FDA) 1
lanley liao Does all of the suppliers need to integrated into the supplier list qualified of the company? Oil and Gas Industry Standards and Regulations 2
0 To which part of 13485 does this refer? ISO 13485:2016 - Medical Device Quality Management Systems 3
A Medical Device Contract Manufacturer - Does the CM need to register with FDA? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
J Records Control - Does each individual record need to be numbered? Records and Data - Quality, Legal and Other Evidence 2
lanley liao Does the customer`s trademark belong to customer-supplied property? Oil and Gas Industry Standards and Regulations 2
H How does a gas turbine work on diesel fuel? Oil and Gas Industry Standards and Regulations 12
G What does performance specification include? US Food and Drug Administration (FDA) 1
W Where does a coatings and paint company fall in IATF? IATF 16949 - Automotive Quality Systems Standard 5
A How much does a complete biocompatibility test package cost? Other ISO and International Standards and European Regulations 1
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 16
C Does an accessory need an IFU if it use is discussed in the Parent device IFU? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
S How long does it take to register a product with MHRA? UK Medical Device Regulations 8
M Quality Manual - Where does Revision History Section go? Document Control Systems, Procedures, Forms and Templates 8

Similar threads

Top Bottom