# Commission Regulation (EU) No 1141/2010 of 7 December 2010 laying down the procedure for the renewal of the inclusion of a second group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances (Text with EEA relevance), Annex II: Format for application, as provided for in Article 5(1)

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Status: repealed

The application shall be in writing, signed by the applicant, and sent by registered mail to the rapporteur Member State listed in column B of Annex I and to the co-rapporteur Member State listed in column C of Annex I.
A copy of the application without the updating statement shall be sent to the European Commission, DG Health and Consumers, unit E3, 1049 Brussels, Belgium and to the Authority, European Food Safety Authority, Largo N. Palli 5/A, 43121 Parma, Italy.
The application shall be submitted in accordance with the following model.
An updating statement, as provided for in Article 5(2), shall be attached as an Annex to the application.
The applicant confirms that the above information submitted on … (date) is correct.
Signature (of the person competent to act for the applicant referred to under 1.1)

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Source: https://www.legislation.gov.uk/eur/2010/1141/annex/II (the official version)
Page: https://openlegislation.uk/eu-regulation-2010-1141/annex-II
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.