# Commission Implementing Regulation (EU) 2017/12 of 6 January 2017 regarding the form and content of the applications and requests for the establishment of maximum residue limits in accordance with Regulation (EC) No 470/2009 of the European Parliament and of the Council (Text with EEA relevance), Division A.3

Extent: E+W+S+N.I.

Toxicology (in laboratory species);
A.3.1.single-dose toxicity, where available;
A.3.2.repeat-dose toxicity;
A.3.2.1.repeat-dose (90-day) oral toxicity testing;
A.3.2.2.repeat-dose (chronic) toxicity testing;
A.3.3.tolerance in target species, where available;
A.3.4.reproductive toxicity, including developmental toxicity;
A.3.4.1.study of the effects on reproduction;
A.3.4.2.study of developmental toxicity;
A.3.5.genotoxicity;
A.3.6.carcinogenicity;

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Source: https://www.legislation.gov.uk/eur/2017/12/annex/chapter/2/division/A/division/A.3 (the official version)
Page: https://openlegislation.uk/eu-regulation-2017-12/annex/chapter-2/division-A/division-A.3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.