# Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006 (Text with EEA relevance), Division 3.4.2.2.3.2

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

Animal test results for sub-category 1A can include data with values indicated in Table 3.4.3
Table 3.4.3
Animal test results for sub-category 1A
Assay
Criteria
Local lymph node assay
EC3 value ≤ 2 %
Guinea pig maximisation test
≥ 30 % responding at ≤ 0,1 % intradermal induction dose or
≥ 60 % responding at > 0,1 % to ≤ 1 % intradermal induction dose
Buehler assay
≥ 15 % responding at ≤ 0,2 % topical induction dose or
≥ 60 % responding at > 0,2 % to ≤ 20 % topical induction dose

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Source: https://www.legislation.gov.uk/eur/2008/1272/annex/I/division/3/division/3.4/division/3.4.2/division/3.4.2.2/division/3.4.2.2.3/division/3.4.2.2.3.2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2008-1272/annex-I/division-3/division-3.4/division-3.4.2/division-3.4.2.2/division-3.4.2.2.3/division-3.4.2.2.3.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.