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2.

The Commission shall in consultation with the Agency forthwith examine the reasons advanced by the Member State concerned. It shall request the opinion of the Committee within a time limit to be determined by the Commission having regard to the urgency of the matter. Whenever practicable, the person responsible for placing the veterinary medicinal product on the market shall be invited to provide oral or written explanations.

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Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.