EN ISO 19238:2017
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Radiological protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics (ISO 19238:2014)
30-04-2018
18-10-2017
European foreword
Foreword
Introduction
1 Scope
2 Terms and definitions
3 Dicentric assay
4 Responsibility of the customer
5 Responsibility of the service laboratory
6 Confidentiality of personal information.
7 Laboratory safety requirements
8 Calibration curve(s)
9 Scoring unstable chromosome aberrations
10 Criteria for converting a measured
aberration frequency into an estimate of
absorbed dose
11 Reporting of results
12 Quality assurance and quality control
Annex A (informative) - Sample instructions for customer
Annex B (informative) - Sample questionnaire
Annex C (informative) - Sample of report
Annex D (informative) - Fitting of the low-LET
dose-response curve by the method of maximum
likelihood and calculating the error of dose estimate
Annex E (informative) - Odds ratio method for cases
of suspected exposure to a low dose
Annex F (informative) - Sample data sheet for
recording aberrations
Bibliography
ISO 19238:2014 provides criteria for quality assurance and quality control, evaluation of the performance, and the accreditation of biological dosimetry by cytogenetic service laboratories.ISO 19238:2014 addressesa) the confidentiality of personal information, for the customer and the service laboratory,b) the laboratory safety requirements,c) the calibration sources and calibration dose ranges useful for establishing the reference dose-effect curves that contribute to the dose estimation from chromosome aberration frequency and the minimum resolvable doses,d) the scoring procedure for unstable chromosome aberrations used for biological dosimetry,e) the criteria for converting a measured aberration frequency into an estimate of absorbed dose,f) the reporting of results,g) the quality assurance and quality control,h) informative annexes containing sample instructions for customer, sample questionnaire, sample of report, fitting of the low dose-response curve by the method of maximum likelihood and calculating the error of dose estimate, odds ratio method for cases of suspected exposure to a low dose, and sample data sheet for recording aberrations.
Committee |
CEN/TC 430
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Withdrawn
|
Standards | Relationship |
ISO 19238:2014 | Identical |
I.S. EN ISO 19238:2017 | Identical |
NEN EN ISO 19238 : 2017 | Identical |
NS EN ISO 19238 : 2017 | Identical |
SN EN ISO 19238:2018 | Identical |
BS EN ISO 19238:2017 | Identical |
PN EN ISO 19238 : 2017 | Identical |
DIN EN ISO 19238:2020-05 | Identical |
NF EN ISO 19238 : 2017 | Identical |
ONORM EN ISO 19238 : 2018 | Identical |
UNI EN ISO 19238 : 2017 | Identical |
DS EN ISO 19238 : 2017 | Identical |
UNE-EN ISO 19238:2018 | Identical |
ISO 5725-1:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions |
ISO/IEC Guide 98-3:2008 | Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995) |
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