Framework for the quality assurance of ’omics technologies considering GLP requirements-Reference-Cited by-同舟云学术

Framework for the quality assurance of ’omics technologies considering GLP requirements

Published:2017-12 Issue: Volume:91 Page:S27-S35
ISSN:0273-2300
Container-title:Regulatory Toxicology and Pharmacology
language:en
Short-container-title:Regulatory Toxicology and Pharmacology

Author:

Kauffmann Hans-Martin,Kamp Hennicke,Fuchs Regine,Chorley Brian N.,Deferme Lize,Ebbels Timothy,Hackermüller Jörg,Perdichizzi Stefania,Poole Alan,Sauer Ursula G.,Tollefsen Knut E.,Tralau Tewes,Yauk Carole,van Ravenzwaay Ben

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference17 articles.

1. Framework for the quantitative weight-of-evidence analysis of ‘omics data for regulatory purposes;Bridges;Regul. Toxicol. Pharmacol.,2017

2. Applying ‘omics technologies in chemicals risk assessment: report of an ECETOC workshop;Buesen;Regul. Toxicol. Pharmacol.,2017

3. European Chemicals Agency. Read-across Assessment Framework (RAAF);ECHA,2015

4. European Medicines Agency ICH Topic S 8 Immunotoxicity Studies for Human Pharmaceuticals;EMA,2006

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