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Laboratory Quality Management Training


Laboratory Quality Management Training

2 Days Training Course on Laboratory Quality Management [ISO 17025:2017] Revision

Understanding the elements of ISO/IEC 17025:2017 & exercise on risk/Sampling Uncertainty

Day 1

One-day training workshop on “Understanding the elements of ISO/IEC 17025:2017” with 6 sets of printed training notes

Course contents :

•        Introducing the concept of laboratory accreditation and international scene

•        Journey towards the new ISO/IEC 17025:2017

•        Transition policy of SAC-SINGLAS

•        Highlights of major changes in the new standard

•        Detailed discussions of the clauses in the new standard

•        In-depth discussions on pertinent topics like sampling and decision rules for risk based thinking 


Day 2:

Course contents:

•        Basic concept of significance testing and analysis of variance

•        Sampling

•        Importance of sampling

•        Newly revised ISO/IEC 17025:2017 requirements

•        Types of sampling and sub-sampling methods

•     Sampling uncertainty

•        Sources of sampling error

•        Approaches for sampling uncertainty estimation

•        Related clauses in the new ISO/IEC 17025:2017

•        What is “risk”?

•        General consideration for risk-based approach

•        Potential quality risk assessment in laboratory operation (e.g., impartiality, independence, validity of test results)

•        Risk assessment methods – qualitative and quantitative

•        What is “conformance testing”?

•        Hypothesis (significance) testing and decision rule

•        Decision rule – definition and on false acceptance/false rejection risks (Type I and Type II errors)

•        Setting tolerance limits to specification

•        OIML Guide 19 methods (classical and probabilistic)

•        An example for decision rules:  Maximum permissible error (MPE) for measurement instruments

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Map E2I Training Room Unit 07-01, 80 Jurong East Street 21, Singapore, Singapore
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