# Commission Implementing Regulation (EU) No 503/2013 of 3 April 2013 on applications for authorisation of genetically modified food and feed in accordance with Regulation (EC) No 1829/2003 of the European Parliament and of the Council and amending Commission Regulations (EC) No 641/2004 and (EC) No 1981/2006 (Text with EEA relevance), Division D: The applicant shall, in addition to the information required under Sections A, B and C provide the following information regarding the testing:

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

1..participating laboratories, time of the analysis and outline of the experimental design, including the details about the number of runs, samples, replicates, etc.;
2..description of the laboratory samples (such as size, quality, date of sampling), positive and negative controls as well as certified reference material, plasmids and alike used;
3..description of the approaches that have been used to analyse the test results and outliers;
4..any particular points observed during the testing;
5..references to relevant literature or technical provisions used in the testing.

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Source: https://www.legislation.gov.uk/eur/2013/503/annex/III/division/3/division/3.2/division/D (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-503/annex-III/division-3/division-3.2/division-D
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.