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I.S. EN ISO 17099:2017

Current

Current

The latest, up-to-date edition.

RADIOLOGICAL PROTECTION - PERFORMANCE CRITERIA FOR LABORATORIES USING THE CYTOKINESIS BLOCK MICRONUCLEUS (CBMN) ASSAY IN PERIPHERAL BLOOD LYMPHOCYTES FOR BIOLOGICAL DOSIMETRY (ISO 17099:2014)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-01-2017

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.


Dates of withdrawal of national standards are available from NSAI.

€59.00
Excluding VAT

National Foreword
European foreword
Foreword
Introduction
1 Scope
2 Terms and definitions
3 Micronucleus assay methodology used in this standard
4 Confidentiality of personal information
5 Laboratory safety requirements
6 Calibration source(s), calibration curve, and minimum
   resolvable dose
7 Responsibility of the customer
8 Responsibility of the CBMN laboratory
9 Accidental overexposure involving few individuals
10 Population triage
11 Quality assurance and quality control
Annex A (informative) - Sample data sheet for recording micronuclei
        in binucleated cells
Annex B (informative) - Automation of micronuclei scoring
Annex C (informative) - Instructions for customer (sample)
Annex D (informative) - Sample questionnaire
Annex E (informative) - Sample of report for single assessment
Annex F (informative) - Example group sample report
Bibliography

Describes the following: a) confidentiality of personal information for the customer and the laboratory; b) laboratory safety requirements; c) radiation sources, dose rates, and ranges used for establishing the calibration reference dose-effect curves allowing the dose estimation from CBMN assay yields and the minimum resolvable dose; d) performance of blood collection, culturing, harvesting, and sample preparation for CBMN assay scoring; e) scoring criteria; f) conversion of micronucleus frequency in binucleated cells into an estimate of absorbed dose; g) reporting of results; h) quality assurance and quality control; and i) informative annexes containing examples of a questionnaire, instructions for customers, a microscope scoring data sheet, a sample report and advice on strengths and limitations of current automated systems for automated micronucleus scoring.

DocumentType
Standard
Pages
48
PublisherName
National Standards Authority of Ireland
Status
Current

Standards Relationship
EN ISO 17099:2017 Identical
ISO 17099:2014 Identical

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