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Guidance on monitoring validity of the results for chemical analysis laboratory
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GB/Z 27426-2022
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Basic data | Standard ID | GB/Z 27426-2022 (GB/Z27426-2022) | | Description (Translated English) | Guidance on monitoring validity of the results for chemical analysis laboratory | | Sector / Industry | National Standard | | Classification of Chinese Standard | A00 | | Classification of International Standard | 03.120.20 | | Word Count Estimation | 22,266 | | Date of Issue | 2022-10-14 | | Date of Implementation | 2022-10-12 | | Issuing agency(ies) | State Administration for Market Regulation, China National Standardization Administration |
GBZ27426-2022: Guidance on monitoring validity of the results for chemical analysis laboratory---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
GB /Z 27426-2022
Guidance on monitoring validity of the results for chemical analysis laboratory
ICS 03.120.20
CCSA00
National Standardization Guiding Technical Document of the People's Republic of China
Guidelines for Monitoring the Validity of Chemical Analysis Laboratory Results
Published on 2022-10-12
2022-10-12 Implementation
State Administration for Market Regulation
Released by the National Standardization Administration
directory
Preface I
Introduction II
1 Scope 1
2 Normative references 1
3 Terms, Definitions and Symbols 1
3.1 Terms and Definitions 1
3.2 Symbol 3
4 General 3
5 Monitoring planning 3
6 Internal Monitoring 4
6.1 Using reference materials/standard samples or quality control samples 4
6.2 Spike recovery7
6.3 Using blank samples 8
6.4 Drawing Control Charts 9
6.5 Verification during equipment period 10
6.6 Repeated Analysis 11
6.7 Intra-lab comparisons 11
6.8 Result correlation analysis 13
7 External monitoring 13
7.1 Proficiency testing 13
7.2 Interlaboratory comparison 14
Appendix A (Informative) Example 16
Reference 19
foreword
This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for Standardization Work Part 1.Structure and Drafting Rules of Standardization Documents"
drafted.
Please note that some content of this document may be patented. The issuing agency of this document assumes no responsibility for identifying patents.
This document is proposed and managed by the National Certification and Accreditation Standardization Technical Committee (SAC/TC261).
This document is drafted by. China National Accreditation Center for Conformity Assessment, National Geological Experiment and Testing Center, Shenzhen Customs Food Inspection and Quarantine Technology
Technology Center, China Petroleum and Chemical Industry Federation, China Petroleum & Chemical Corporation Petrochemical Research Institute, China Medical Science
Institute of Pharmacy, China Standard Technical Service (Shanghai) Co., Ltd., Institute of Testing and Analysis of Guangdong Academy of Sciences (Guangzhou, China Analysis and Testing
Center), Industrial Analysis and Testing Center of Guangdong Academy of Sciences, China Certification and Accreditation Association, National Environmental Analysis and Testing Center, Steel Research Nanogram Testing Technology
Technology Co., Ltd.
The main drafters of this document. Zhao Bingnan, Wang Suming, Wang Shanshan, Sun Peiqin, Dong Fuyin, Wei Jing, Zhou Yongyun, Yang He, Ma Yuan, Zhang Jinlan,
Liu Fufang, Wu Huiqin, Ma Yanfang, Wang Yaning, Du Bing, Hu Jingyu, He Zhaowei.
Introduction
Chemical analysis involves many industries and fields such as chemical industry, petroleum, geology, environment, food and medicine, and the validity of laboratory test results is monitored
especially important. With the wide application of the international standard ISO /IEC 17025 and the continuous enhancement of laboratory quality awareness, laboratory managers have
More and more attention has been paid to the monitoring of the validity of the test results, and the monitoring of the validity of the test results has become an important part of laboratory management. Although
ISO /IEC 17025 gives general requirements for laboratories to ensure the validity of results, and applies to all testing laboratories carrying out test results with
The organization and management of effectiveness monitoring, however, due to the uneven level of laboratory capacity, many laboratories are carrying out results effectiveness monitoring and management.
There is still a lot of confusion.
According to the technical characteristics of chemical analysis laboratories, this document clarifies the general principles of monitoring and management of the effectiveness of results, and guides the risk-based
The basic method of analyzing and evaluating results is used for monitoring and planning, and the selection and evaluation of internal monitoring methods, external monitoring methods and their results are given.
The specific guidance for application is aimed at improving the quality of laboratory test results and improving the validity and reliability of laboratory test results.
Guidelines for Monitoring the Validity of Chemical Analysis Laboratory Results
1 Scope
This document provides general principles, monitoring planning, internal and external monitoring methods and implementation requirements for the effectiveness of monitoring results in chemical analysis laboratories.
Points and results evaluation and other guidance.
This document is intended to guide the monitoring of the validity of chemical analysis laboratory results.
2 Normative references
The contents of the following documents constitute essential provisions of this document through normative references in the text. Among them, dated citations
documents, only the version corresponding to that date applies to this document; for undated references, the latest edition (including all amendments) applies to
this document.
GB/T 6379.1-2004 Accuracy (correctness and precision) of measurement methods and results - Part 1.General provisions and definitions
GB/T 15000.2-2019 Working Guidelines for Standard Samples Part 2.Common Terms and Definitions
GB/T 19000-2016 Quality Management System Fundamentals and Terminology
GB/T 27025-2019 General requirements for the competence of testing and calibration laboratories
JJF1001-2011 General Metrology Terms and Definitions
JJF1033-2016 Measurement Standard Assessment Specification
JJF1059.1-2012 Evaluation and representation of measurement uncertainty
3 Terms, Definitions and Symbols
GB/T 6379.1-2004, GB/T 15000.2-2019, GB/T 19000-2016, JJF1001-2011, JJF1033-2016
Terms and definitions defined in JJF1059.1-2012 apply to this document. For convenience, this document repeats the following terms and definitions.
3.1 Terms and Definitions
3.1.1
effectiveness
The extent to which planned activities are completed and planned results are obtained.
[Source. GB/T 19000-2016, 3.7.11]
3.1.2
calibration
A set of operations under specified conditions, the first step of which is to determine the relationship between the magnitude provided by the measuring standard and the corresponding indication, the second step
It is to use this information to determine the relationship between the measurement results obtained from the indication value, where both the quantity provided by the measurement standard and the corresponding indication value have measurement uncertainty.
fixed.
[Source. JJF1001-2011, 4.10]
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