Traduction de «advice about any matters relating » (Néerlandais → Français) :

It may formulate advice about any matters relating to the policies being followed or to be pursued by the FAMHP. This committee consists of representatives of patients and users, of all sectors who are involved in the matters under the Agency’s mission, as well as representatives from the relevant federal public services.
It may formulate advice about any matters relating to the policies being followed or to be pursued by the FAMHP. This committee consists of representatives of patients and users, of all sectors who are involved in the matters under the Agency’s mission, as well as representatives from the relevant federal public services.

This release contains forward-looking information about an agreement by Pfizer to acquire FoldRx, and about FoldRx’s product candidate tafamidis, its other clinical and preclinical development programs and its technology platform, including their potential benefits, that involves substantial risks and uncertainties. Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009 and in its reports on Form 10-Q and Form 8-K.
Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments.

The official role of this commission is to issue advice to determine the status of products when there is any doubt or uncertainty about whether or not they are medicines.
The official role of this commission is to issue advice to determine the status of products when there is any doubt or uncertainty about whether or not they are medicines.