33In the third place, in accordance with the first paragraph of Article 62(1) of Regulation No 726/2004, where the Committee is required to evaluate a medicinal product for human use, it is to appoint one of its members to act as rapporteur and may appoint a second member to act as co-rapporteur. The role of rapporteur entails taking on an important role in preparing the opinion which the Committee is called upon to issue.
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