Vertaling van "from the relevant federal public " (Nederlands → Frans) :

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.

The FAMHP was established by law on 20 July 2006 and as from 1 January 2007 completely took over the role and fields of competency of the Directorate-General for Medicinal Products (DG Medicinal Products) that was a part of the Federal Public Service (FPS) Public Health, Food Chain Security and Environment.
The FAMHP was established by law on 20 July 2006 and as from 1 January 2007 completely took over the role and fields of competency of the Directorate-General for Medicinal Products (DG Medicinal Products) that was a part of the Federal Public Service (FPS) Public Health, Food Chain Security and Environment.

In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.
In order to regulate the quality and relevance of messages to the public, a prior licence is required for radio and TV information campaigns about human health and illness which refer directly or indirectly to medicines. This licence is normally issued by the Minister responsible following advice from the Commission for the supervision of advertising for medicines for human use.