2.

At the time of application, the applicant shall send the following particulars and documents directly to the Authority: a copy of the authorisation for placing the feed additive on the market; a report on the results of the post-market monitoring, if such monitoring requirements are included in the authorisation; any other new information which has become available with regard to the evaluation of the safety in use of the feed additive and the risks of the feed additive to animals, humans or the environment; where appropriate, a proposal for amending or supplementing the conditions of the original authorisation, inter alia, the conditions concerning future monitoring.

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Source: EUR-Lex (Cellar) · retrieved 2026-11-02 · Text as adopted (Official Journal); later amendments are not incorporated in this text.