# 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 1.11

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

Where the micro-organism has been genetically modified, as defined in Directive 2001/18/EC, no authorisation shall be granted unless the evaluation conducted in accordance with the EU-derived domestic legislation which transposed Directive 2001/18/EC has been submitted, as required pursuant to Article 53(4) of Regulation (EC) No 1107/2009. The relevant decision taken by the competent authorities in accordance with the EU-derived domestic legislation which transposed Directive 2001/18/EC must be provided.

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Source: https://www.legislation.gov.uk/eur/2011/546/annex/part/II/division/C/division/1/division/1.11 (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-546/annex/part-II/division-C/division-1/division-1.11
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

