34It should be noted, first, that, under Directive 2001/83, the procedure for the granting of a MA is conceived as a bilateral procedure involving only the applicant and the competent authority (see, by analogy, judgment in Olivieri v Commission and EMEA, T‑326/99, EU:T:2003:351, paragraph 94) and that that directive does not contain any express provision to the effect that a judicial remedy is available to the holder of a MA granted for an original medicinal product to challenge the decision of the competent authority which granted, pursuant to Article 10 of the directive, a MA for a generic medicinal product for which the original product served as the reference product.
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