# Commission Regulation (EU) 2018/782 of 29 May 2018 establishing the methodological principles for the risk assessment and risk management recommendations referred to in Regulation (EC) No 470/2009 (Text with EEA relevance), Division II.6.3.3.2.2

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

The data from chronic oral toxicity testing studies shall allow:
(a)the evaluation of the functional and morphological changes due to repeated administration of the test substance(s) and how these changes are related to dose;
(b)the establishment of a NO(A)EL or LO(A)EL or BMDL.

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Source: https://www.legislation.gov.uk/eur/2018/782/annex/I/division/II/division/II.6/division/II.6.3/division/II.6.3.3/division/II.6.3.3.2/division/II.6.3.3.2.2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2018-782/annex-I/division-II/division-II.6/division-II.6.3/division-II.6.3.3/division-II.6.3.3.2/division-II.6.3.3.2.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.