# Commission Regulation (EU) No 544/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances (Text with EEA relevance) (repealed), Division (i): The information provided, taken together with that provided for one or more preparations containing the active substance, must be sufficient to permit an evaluation to be made as to the risks for man, arising from residues of the active substance and relevant metabolites, degradation and reaction products remaining in food. In addition, the information provided must be sufficient to:

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

permit a decision to be made as to whether, or not, the active substance can be approved,
specify appropriate conditions or restrictions to be associated with any approval.

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Source: https://www.legislation.gov.uk/eur/2011/544/annex/part/A/division/6/division/1/division/i (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-544/annex/part-A/division-6/division-1/division-i
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.