NF ISO 12787

NF ISO 12787

February 2012
Standard Current

Cosmetics - Analytical methods - Validation criteria for analytical results using chromatographic techniques

ISO 12787:2011 defines validation criteria with which analytical results obtained from the analysis of cosmetic products should comply in order to give confidence in performance, reliability and quality of the final result. It sets out an analytical approach that can be used by a single laboratory to carry out chromatographic analyses on a given sample, or samples.

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Main informations

Collections

National standards and national normative documents

Publication date

February 2012

Number of pages

22 p.

Reference

NF ISO 12787

ICS Codes

71.100.70   Cosmetics. Toiletries

Classification index

T75-612

Print number

1 - 10/02/2012

International kinship

Sumary
Cosmetics - Analytical methods - Validation criteria for analytical results using chromatographic techniques

ISO 12787:2011 defines validation criteria with which analytical results obtained from the analysis of cosmetic products should comply in order to give confidence in performance, reliability and quality of the final result. It sets out an analytical approach that can be used by a single laboratory to carry out chromatographic analyses on a given sample, or samples.

Table of contents
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  • Avant-propos
    iv
  • 1 Domaine d'application
    1
  • 2 Termes et définitions
    1
  • 2.1 Généralités
    1
  • 2.2 Termes relatifs aux critères de validation pour les résultats analytiques
    2
  • 3 Principe
    4
  • 4 Informations générales
    4
  • 4.1 Effet matrice
    4
  • 4.2 Arbre décisionnel
    5
  • 5 Première étape - Critères de validation minimaux sur les solutions étalons
    6
  • 5.1 Généralités
    6
  • 5.2 Estimation des limites de détection et de quantification dans le solvant (étape facultative)
    7
  • 5.3 Conformité analytique
    7
  • 5.4 Étalonnage: fidélité, linéarité et exactitude
    8
  • 6 Deuxième étape - Criblage de l'échantillon
    9
  • 6.1 Généralités
    9
  • 6.2 Criblage de l'échantillon
    9
  • 7 Troisième étape - Dosages
    9
  • 7.1 Généralités
    9
  • 7.2 Analytes non détectés ou détectés à des concentrations inférieures à la LoQ
    10
  • 7.3 Analytes détectés à une concentration supérieure à la LoQ
    10
  • 8 Conclusion
    12
  • Annexe A (informative) Exemple de choix du coefficient de pondération
    14
  • Annexe B (normative) Dosages avec une valeur cible (approche simplifiée)
    15
  • Bibliographie
    16
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