# Commission Regulation (EU) No 546/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards uniform principles for evaluation and authorisation of plant protection products (Text with EEA relevance), Division 1.13

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

No authorisation shall be granted if relevant metabolites/toxins (i.e. those expected to be of concern for human health and/or the environment) known to be formed by the micro-organism, and/or by microbial contaminants are present in the plant protection product, unless it can be shown that the amount present is at an acceptable level before and after its proposed use.

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Source: https://www.legislation.gov.uk/eur/2011/546/annex/part/II/division/C/division/1/division/1.13 (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-546/annex/part-II/division-C/division-1/division-1.13
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

