@article{Krebs2020-07EUTox-50516,
  year={2020},
  doi={10.1007/s00204-020-02802-6},
  title={The EU-ToxRisk method documentation, data processing and chemical testing pipeline for the regulatory use of new approach methods},
  number={7},
  volume={94},
  issn={0340-5761},
  journal={Archives of Toxicology},
  pages={2435--2461},
  author={Krebs, Alice and van Vugt-Lussenburg, Barbara M. A. and Waldmann, Tanja and Busquet, Francois and Dolde, Xenia and Holzer, Anna-Katharina and Kisitu, Jaffar and Pallocca, Giorgia and Rovida, Costanza and Leist, Marcel}
}

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    <dc:contributor>Krebs, Alice</dc:contributor>
    <dc:creator>Kisitu, Jaffar</dc:creator>
    <dc:contributor>Waldmann, Tanja</dc:contributor>
    <dc:contributor>Busquet, Francois</dc:contributor>
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    <dcterms:abstract xml:lang="eng">Hazard assessment, based on new approach methods (NAM), requires the use of batteries of assays, where individual tests may be contributed by different laboratories. A unified strategy for such collaborative testing is presented. It details all procedures required to allow test information to be usable for integrated hazard assessment, strategic project decisions and/or for regulatory purposes. The EU-ToxRisk project developed a strategy to provide regulatorily valid data, and exemplified this using a panel of &gt; 20 assays (with &gt; 50 individual endpoints), each exposed to 19 well-known test compounds (e.g. rotenone, colchicine, mercury, paracetamol, rifampicine, paraquat, taxol). Examples of strategy implementation are provided for all aspects required to ensure data validity: (i) documentation of test methods in a publicly accessible database; (ii) deposition of standard operating procedures (SOP) at the European Union DB-ALM repository; (iii) test readiness scoring accoding to defined criteria; (iv) disclosure of the pipeline for data processing; (v) link of uncertainty measures and metadata to the data; (vi) definition of test chemicals, their handling and their behavior in test media; (vii) specification of the test purpose and overall evaluation plans. Moreover, data generation was exemplified by providing results from 25 reporter assays. A complete evaluation of the entire test battery will be described elsewhere. A major learning from the retrospective analysis of this large testing project was the need for thorough definitions of the above strategy aspects, ideally in form of a study pre-registration, to allow adequate interpretation of the data and to ensure overall scientific/toxicological validity.</dcterms:abstract>
    <dc:contributor>Holzer, Anna-Katharina</dc:contributor>
    <dc:contributor>Rovida, Costanza</dc:contributor>
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    <dc:creator>van Vugt-Lussenburg, Barbara M. A.</dc:creator>
    <dc:contributor>van Vugt-Lussenburg, Barbara M. A.</dc:contributor>
    <dc:creator>Holzer, Anna-Katharina</dc:creator>
    <dc:contributor>Dolde, Xenia</dc:contributor>
    <dc:creator>Pallocca, Giorgia</dc:creator>
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    <dc:creator>Waldmann, Tanja</dc:creator>
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