NF ISO 19238

NF ISO 19238

December 2005
Standard Cancelled

Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics

ISO 19238:2004 provides criteria for quality assurance and quality control, evaluation of the performance and the accreditation of biological dosimetry by cytogenetic service laboratories.

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Main informations

Collections

National standards and national normative documents

Thematics

Sécurité, Gestion des risques et SST, QSE

Publication date

December 2005

Number of pages

28 p.

Reference

NF ISO 19238

ICS Codes

13.280   Radiation protection
17.240   Radiation measurements

Classification index

M60-220

Print number

1 - 14/11/2005

International kinship

Sumary
Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics

ISO 19238:2004 provides criteria for quality assurance and quality control, evaluation of the performance and the accreditation of biological dosimetry by cytogenetic service laboratories.

Standard replaced by (1)
NF ISO 19238
April 2014
Standard Cancelled
Radiation protection - Performance criteria for service laboratories performing biological dosimetry by cytogenetics

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 addresses a) 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.

Table of contents
  • Avant-propos
    v
  • Introduction
    vi
  • 1 Domaine d'application
    1
  • 2 Termes et définitions
    1
  • 3 Dénombrement des dicentriques
    3
  • 4 Confidentialité des informations personnelles
    4
  • 4.1 Généralités
    4
  • 4.2 Applications du principe de confidentialité
    4
  • 5 Exigences de sécurité du laboratoire
    5
  • 5.1 Généralités
    5
  • 5.2 Exigences de sécurité microbiologique
    5
  • 5.3 Exigences de sécurité chimique
    5
  • 5.4 Exigences de sécurité optique
    7
  • 5.5 Procédures de sécurité
    7
  • 6 Source(s) d'étalonnage, courbes(s) d'étalonnage et seuils de détection
    7
  • 6.1 Source(s) d'étalonnage
    7
  • 6.2 Courbe(s) d'étalonnage
    7
  • 6.3 Seuils limite de détection
    7
  • 7 Responsabilité du demandeur
    8
  • 8 Responsabilité du laboratoire de service
    8
  • 9 Dénombrement des aberrations chromosomiques instables
    9
  • 9.1 Procédure pour l'analyse des métaphases en première division
    9
  • 9.2 Critères pour le dénombrement
    9
  • 10 Critères pour convertir une fréquence d'aberration mesurée en une estimation de dose absorbée
    10
  • 10.1 Généralités
    10
  • 10.2 Comparaison avec les valeurs témoins
    10
  • 10.3 Détermination de l'estimation de dose et des limites de l'intervalle de confiance
    10
  • 10.4 Cas d'exposition aiguë et non aiguë
    11
  • 10.5 Cas d'exposition hétérogène ou ancienne
    11
  • 11 Compte rendu des résultats
    11
  • 11.1 Identification du sujet exposé
    11
  • 11.2 Description du cas
    12
  • 11.3 Obligations du laboratoire de service
    12
  • 11.4 Résultats du laboratoire de service
    12
  • 11.5 Interprétation des résultats
    12
  • 11.6 Responsable du rapport
    12
  • 11.7 Résumé
    12
  • 12 Assurance de la qualité et contrôle de la qualité
    13
  • 12.1 Généralités
    13
  • 12.2 Assurance de la qualité
    13
  • 12.3 Contrôle de la qualité
    15
  • Annexe A (informative) Instructions pour le demandeur (exemple)
    17
  • Annexe B (informative) Exemple de questionnaire
    18
  • Annexe C (informative) Tableau type pour le dénombrement des aberrations chromosomiques
    20
  • Annexe D (informative) Exemple de rapport
    21
  • Bibliographie
    22
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