Vertaling van "medicinal products official journal " (Nederlands → Frans) :

European Parliament and Council Regulation (EC) No 141/2000 of 16 December 1999, on orphan medicinal products [Official Journal L 18 of 22.01.2000].
Règlement (CE) n o 141/2000 du Parlement européen et du Conseil, du 16 décembre 1999, concernant les médicaments orphelins, JO L 18 du 22 janvier 2000, pp.0001-0005 ( [http ...]

The latter has been designated as having expertise as an “Official Medicines Control Laboratory”, recognised by the FAMHP and the European Directorate for the Quality of Medicines (EDQM), for the monitoring of immunological products for veterinary use prior to marketing authorisation for the Belgian market.
The latter has been designated as having expertise as an “Official Medicines Control Laboratory”, recognised by the FAMHP and the European Directorate for the Quality of Medicines (EDQM), for the monitoring of immunological products for veterinary use prior to marketing authorisation for the Belgian market.

The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).
The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).

The Belgian Federal Agency for Medicines and Health Products (FAMHP) was officially created on 1 January 2007.
The Belgian Federal Agency for Medicines and Health Products (FAMHP) was officially created on 1 January 2007.

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.