http://www.legislation.gov.uk/eur/2012/528/annex/IV/division/1/division/1.3/2020-12-31Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance)Regulation (EU) No 528/2012 of the European Parliament and of the CouncilRegulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance)King's Printer of Acts of Parliamenthttps://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02012R0528-20191120texttext/xmlen2024-07-31Expert Participation2020-12-31 ANNEX IV <Strong>GENERAL RULES FOR THE ADAPTATION OF THE DATA REQUIREMENTS</Strong> 1.TESTING DOES NOT APPEAR SCIENTIFICALLY NECESSARY1.3.Qualitative or Quantitative structure-activity relationship ((Q)SAR)

Results obtained from valid qualitative or quantitative structure-activity relationship models ((Q)SARs) may indicate the presence, but not the absence of a given dangerous property. Results of (Q)SARs may be used instead of testing when the following conditions are met:

the results are derived from a (Q)SAR model whose scientific validity has been established,the substance falls within the applicability domain of the (Q)SAR model,the results are adequate for the purpose of classification and labelling and risk assessment, andadequate and reliable documentation of the applied method is provided.

...

Words in Annex 4 para. 1.3 omitted (31.12.2020) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 142(b); 2020 c. 1, Sch. 5 para. 1(1)
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