Documente Academic
Documente Profesional
Documente Cultură
Punyam
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Punyam
MESSAGE
Click toFROM ISO/IECtitle
edit Master 17025:2017
style
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MESSAGE IN 5 LINES FOR LABORATORIES
Click to edit Master text styles
Click
Say what
Second to edit
you do Master text styles
level
Do what you say
Second
Third
Record
level
level
what you do
Third
Check level
theFourth level
difference
Fourth Fifth level
Act on the level
difference
Fifth
MESSAGE levelIN 1 LINE
Do right thing, first time, every time to Achieve Consistent
Quality
MESSAGE IN 1 LINE
Continual improvement is the way of life
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4.1 Click to edit Master text styles 7.1 Review of 7.2 Selection, 8.1 Options
Second6.1level
Impartiality General requests, tenders
and contracts
verification
and validation
Second Third level
level
of methods 8.2 Management
system
8.3 Control of
management
system documents
4.2 6.2 Personnel 7.4 Handling of documentation
Thirdlevel
Confidentiality Fourth level 7.3 Sampling test or calibration
items
(Option A) (Option A)
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4 TIER DOCUMENTATION STRUCTURE FOR Punyam
Click to editUNDER
LABORATORY Master title
ISO/IEC style
17025:2017
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Click to edit Master Lab text styles
Quality
Click to edit
Second level Master text styles
Manual
Second level
Third level
Thirdlevel
Fourth level Procedures
Fifth level
Fourth level
Fifth level standards/Test
Work Instruction/SOP/ test
Methods/other
documents
Forms/Records
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Click
Click
to edit Master title style
to
The objective ofedit Master
this presentation
an QMS is established in terms of:
title
are to appreciatestyle
and understand how
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Application for Accreditation (by
Laboratory)
Accreditation Procedure
Acknowledgement & Scrutiny of Application
(by accreditation body Secretariat)
Feedback
to
Adequacy of Quality Manual (by Laboratory
Lead Assessor)
6. Closing Meeting
7. Audit report
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ISO/IEC 17025 Accreditation Steps For accredited laboratories
Steps to update existing ISO/IEC 17025:2005 system to revised ISO/IEC 17025:2017
laboratory management system (Existing accredited laboratories)
Conduct awareness program for revision to ISO/IEC 17025:2017
Review all documents to meet revised ISO/IEC 17025:2017 requirements and Identify changes.
Promote the use of risk based thinking and determine risk and opportunities
Review quality policy and establish quality objectives as well as prepare risk sheet
Revise Quality Manual and prepare documents as per revised ISO/IEC 17025:2017.
Train internal auditors for requirements of revised ISO/IEC 17025:2017 standard
Assess the system through internal audit as per revised ISO/IEC 17025:2017 standard.
Take corrective actions on identified non-conformities.
Apply to revised existing certificate to ISO/IEC 17025:2017 standard to your existing accreditation
body.
Final audit (Either in surveillance audit or special audit by accreditation body on ISO/IEC
17025:2017
Note: Also all accredited laboratories needs to update the system within 3 year of release of
standard.
The ISO/IEC 17025:2017 is released in November 2017, the accredited laboratories may
go for Upgradation to ISO/IEC 17025:2017 before November 2020