# Commission Implementing Regulation (EU) No 414/2013 of 6 May 2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance), Article 2: Content of applications

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

By way of derogation from Article 20(1) of Regulation (EU) No 528/2012 ... an application for authorisation of a same product shall contain the following information:
(a)the authorisation number or, for not yet approved related reference products, the application number of the related reference product provided by the competent authority on submission of that application;
(b)an indication of the proposed differences between the same product and the related reference product, and evidence that the products are identical on all other aspects;
(c)where required by Article 59(1) of Regulation (EU) No 528/2012, letters of access to all the data supporting the authorisation of the related reference product;
(d)a draft summary of the biocidal product characteristics for the same product.

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Source: https://www.legislation.gov.uk/eur/2013/414/article/2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2013-414/article-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.