Vertaling van "authorisation " (Nederlands → Frans) :

The FAMHP’s Marketing authorisation Department is responsible for evaluating new applications and requests for amendments to existing marketing authorisation (MA) with a view to granting authorisation for marketing a medicine or health product.
The FAMHP’s Marketing authorisation Department is responsible for evaluating new applications and requests for amendments to existing marketing authorisation (MA) with a view to granting authorisation for marketing a medicine or health product.

The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.
The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.

Een andere bijzonderheid voor het jaar 2009, in het kader van de verwerking van de VHB-dossiers, is de effectieve opsplitsing van het oude Departement Registratie in twee afdelingen: de Afdeling Marketing Authorisation (humaan) van het DG PRE vergunning en de Afdeling Marketing Authorisation – Variaties & Hernieuwingen van het DG POST vergunning.
Une autre particularité de l’année 2009 pour le traitement des dossiers d’AMM est la scission effective de l’ancien Département Enregistrement en deux divisions : la Division Marketing Authorisation (humain) de la DG PRE autorisation et la Division Marketing Authorisation – Variations & Renouvellements de la DG POST autorisation.

Procedure regarding application to authorise or extend authorisation of a cell and tissue bank.
Procedure regarding application to authorise or extend authorisation of a cell and tissue bank.

The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).
The Registration (marketing authorisation) department for its part is required to evaluate applications for a marketing authorisation (MA), for the sake of the National Procedure (NP), the European Decentralised Procedure (DCP), the Mutual Recognition Procedure (MRP) and the Central Procedure (CP).

In 2007, 88 licences/registrations were issued to market participants For the export of precursors, 200 export authorisations and 11 import authorisations were issued.
In 2007, 88 licences/registrations were issued to market participants For the export of precursors, 200 export authorisations and 11 import authorisations were issued.

In 1995, the Council was consulted by the Food Inspection of the Ministry of Public Health in connection with a request from the firm that marketed “Red Bull” regarding the modification of the authorised content of an additive that was already on the list of authorised additives, viz. caffeine.
en 1995, le Conseil est consulté par l’Inspection des denrées alimentaires du Ministère de la Santé publique suite à une demande de la firme commercialisant le Red Bull pour envisager la modification de la teneur autorisée d’un additif déjà inscrit sur la liste d’additifs autorisés, en l’occurrence la caféine.

* * * The situation in Belgium does not differ from that in other European countries as far as the authorisation to market various energy drinks is concerned.
* * * La situation en Belgique n’est pas différente de celle d’autres pays européens en ce sens que la commercialisation de plusieurs boissons énergisantes est tolérée.

In Belgium, the commercialisation of these products has been authorised for over ten years.
En Belgique, leur commercialisation est tolérée depuis plus de 10 ans.

- MA: marketing authorisation: alle doseringen en farmaceutische vormen
- MA : autorisation de mise sur le marché : tous les dosages et toutes les