This collaboration aims to commitments to realize the FAMHP has compared the EMEA, the European Agency for the registration of medicines. The FAMHP CHMP gives its members the task to be rapporteur for some drugs. Zo''n rapporteur ship involves a number of tasks that can be divided broadly into quality, toxicology, and efficacy and safety. The quality section should be done to evaluate the original application for registration or an application for change in manufacturing, control methods and shelf-life of the active ingredient or finished product. The Belgian CHMP members are different files for draftsman in which the medicinal products are produced bio-technology. As Prof. DEFORCE is a biotechnology expert, FAMHP wants to make use of his expertise to perform the tasks mentioned above.