37Since, as stated in recital 23 of Regulation No 726/2004, ‘exclusive responsibility for preparing the [EMA]’s opinions on all questions concerning medicinal products for human use should be vested in a Committee for Medicinal Products for Human Use’ and not in the individual members of that committee, in general, no account may be taken of the ‘Updated (co)-Rapporteurs Joint Assessment Report of the Grounds for the Re-examination Procedure’ of 11 October 2017, which, as the applicant claims, was circulated to all CHMP members on 5 November 2017 as the ‘final assessment report’.
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