Scientific evaluations of data relating to the clinical development of vaccines against tropical diseases submitted to the FAMHP in support of an application for a clinical study, a scientific opinion, a marketing authorisation or a variation of a marketing authorisation.

- Write clinical data evaluation reports for vaccines against tropical diseases,

- Participate in meetings within the FAMHP, in particular with the FAMHP's internal evaluators, with a view to harmonizing evaluations and exchanging information that may be relevant for evaluations.

- Where appropriate, present the assessment report to the committees or working groups of the European Medicines Agency (EMA).

- Participate in meetings with the applicant for national scientific opinions.