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Traduction de «authorisation to market various » (Néerlandais → Français) :

* * * 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.


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.


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).


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.


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.


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.


Borderline products and medicines without a market authorisation The trade in traditional medicines such as TCM (Traditional Chinese Medicines, Ayurveda and others) The theft of medicines and their resale on the black market

Borderline products and medicines without a market authorisation The trade in traditional medicines such as TCM (Traditional Chinese Medicines, Ayurveda and others) The theft of medicines and their resale on the black 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 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.


EC Volume 9 2001 Notice to Marketing Authorisation Herziening wordt uiterlijk in april 2005 Holders vrijgegeven voor openbare raadpleging

EC Volume 9 2001 Notice to Marketing Authorisation Révision à publier pour consultation Holders publique d’ici avril 2005




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Date index: 2022-11-15
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