# Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market (Text with EEA relevance), Division 1.6: The simultaneous use of the active substance as a biocide or in veterinary medicine shall be reported.

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

If the applicant for the active substance in the plant protection product is identical to the one responsible for the notification of the active substance as a biocide or as a veterinary medicine, a summary of all relevant data submitted for approval of the biocide or the veterinary medicine, shall be submitted. This summary shall include toxicological reference values and MRL proposals, taking into account any possible cumulative exposure due to different uses of the same substance based on scientific methods accepted by the ... competent authorities, together with a summary of the residues and toxicology data and information on the use of the product.
If the applicant for the active substance in the plant protection product is not identical to the one responsible for the notification of the active substance as a biocide or in veterinary medicine, a summary of all available data shall be submitted.

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Source: https://www.legislation.gov.uk/eur/2013/283/annex/division/INTRODUCTION/division/1/division/1.6 (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-283/annex/division-INTRODUCTION/division-1/division-1.6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.