GB/T 27420-2018 Active National standards

GB/T 27420-2018 Conformity assessment—Application guide for evaluation and expression of uncertainty in biological sample measurement

GB/T 27420-2018 Conformity assessment—Application guide for evaluation and expression of uncertainty in biological sample measurement

Publish Date: 2018-05-14 Implement Date: 2018-12-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: GB/T 27420-2018
Standard Type: National standards
Standard Status: Active
is_force_gb: no
CCS Name: Standardized management and general provisions
ICS Name: Product certification, institutional certification, and conformity assessment
Publish Date: 2018-05-14
Implement Date: 2018-12-01
Pages: 60 pages

Scope

This standard is an application guide for the evaluation and presentation of the uncertainty of quantitative measurement results of biological samples in the field of conformity assessment. This standard applies to the evaluation of the uncertainty of detection results related to the measurement process, but does not include the impact of biological variability and pre- and post-measurement processes on the measurement results.

Development Information

Word Count: 112 Thousand words Pages: 60 pages

Referenced Standards

ISO 80000-1 GB/T 8170-1987 Rules for rounding off of numberical values GB/T 8170-2008 Rules of rounding off for numerical values & expression and judgement of limiting values GB/T 19702-2005 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Presentation of reference measurement procedures GB/T 19702-2021 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for content and presentation of reference measurement procedures GB/T 21415-2008 In vitro diagnostic medical devices—Measurement of quantities in biological samples—Metrological traceability of values assigned to calibrators and control materials GB/T 21919-2008 Laboratory medicine—Requirements for reference measurement laboratories GB/T 21919-2022 Laboratory medicine—Requirements for the competence of calibration laboratories using reference measurement procedures GB/T 22576-2008 Medical laboratories—Particular requirements for quality and competence GB/T 22576.1-2018 Medical laboratories—Requirements for quality and competence—Part 1:General requirements GB/T 22576.2-2021 Medical laboratories—Requirements for quality and competence—Part 2:Requirements in the field of clinical hematological examination GB/T 22576.3-2021 Medical laboratories—Requirements for quality and competence—Part 3:Requirements in the field of urine examination GB/T 22576.4-2021 Medical laboratories—Requirements for quality and competence—Part 4:Requirements in the field of clinical chemistry examination GB/T 22576.5-2021 Medical laboratories—Requirements for quality and competence—Part 5:Requirements in the field of clinical immunology examination GB/T 22576.6-2021 Medical laboratories—Requirements for quality and competence—Part 6:Requirements in the field of clinical microbiological examination GB/T 22576.7-2021 Medical laboratories—Requirements for quality and competence—Part 7:Requirements in the field of transfusion medicine GB/T 27025-2008 General requirements for the competence of testing and calibration laboratories GB/T 27025-2019 General requirements for the competence of testing and calibration laboratories GB/T 27407-2010 Quality control in laboratories—Applying statistical quality assurance and control charting techniques to evaluate analytical measurement system performance GB/T 27411-2012 Routine methods for evaluation and expression of measurement uncertainty in testing laboratory GB/T 21415-2025 In vitro diagnostic medical devices—Requirements for establishing metrological traceability of values assigned to calibrators,trueness control materials and human samples GB/T 22576.1-2026 Medical laboratories—Requirements for quality and competence—Part 1:General requirements

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