5.

In the event of an opinion in favour of authorising the feed, the opinion shall also include the following particulars: the name and address of the applicant; the designation of the feed, and its specification; where applicable, the information required under Annex II to the Cartagena Protocol; the proposal for the labelling of the feed; where applicable, any conditions or restrictions which should be imposed on the placing on the market and/or specific conditions or restrictions for use and handling, including post-market monitoring requirements based on the outcome of the risk assessment and, in the case of GMOs or feed containing or consisting of GMOs, conditions for the protection of particular ecosystems/environment and/or geographical areas; the method, validated by the Community reference laboratory, for detection, including sampling, identification of the transformation event and, where applicable, for the detection and identification of the transformation event in the feed and/or in feed produced from it; an indication of where appropriate reference material can be accessed; where appropriate, the monitoring plan as referred to in Article 17(5)(b).

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Source: EUR-Lex (Cellar) · retrieved 2026-11-04 · Text as adopted (Official Journal); later amendments are not incorporated in this text.