Vertaling van "manufacturer markets " (Nederlands → Frans) :

TERMINOLOGIE

tandheelkundig 'chairside'-systeem voor CAD (computer-aided design) en CAM (computer-aided manufacturing)
fauteuil de système de CAO/FAO dentaire

tandheelkundig systeem voor CAD (computer-aided design) en CAM (computer-aided manufacturing) vervaardigd in laboratorium
laboratoire de système de CAO/FAO dentaire

applicatiesoftware voor tandheelkundig CAD/CAM (computer-aided design / computer-aided manufacturing)-systeem
logiciel de CAO/FAO

IN-CONTEXT TRANSLATIONS

The manufacturer markets them after simple notification.
The manufacturer markets them after simple notification.

This agreement provides for an enhanced collaboration between the two institutions in the evaluation of quality data in applications for MA or associated amendments (variations) for vaccines for veterinary use, “Good Manufacturing Practices” inspection (GMP) and post-marketing reviews (monitoring by the FAMHP on samples taken).
This agreement provides for an enhanced collaboration between the two institutions in the evaluation of quality data in applications for MA or associated amendments (variations) for vaccines for veterinary use, “Good Manufacturing Practices” inspection (GMP) and post-marketing reviews (monitoring by the FAMHP on samples taken).

Under the new agreement, Novartis received a one-time payment of USD 200 million, principally for manufacturing facilities transferred to Bayer Schering, as well as receiving rights to market a Novartis-branded version of Betaseron ® called Extavia starting in 2009 in the EU and later in the US following anticipated approval.
En vertu de ce nouvel accord, Novartis a reçu un paiement unique d’USD 200 millions, principalement pour le transfert de sites de production à Bayer Schering ainsi que les droits de commercialisation sous la marque Novartis d’une version Betaseron ® appelée Extavia débutant en 2009 en Europe et plus tard au cours de l’année aux Etats-Unis à la suite de l’autorisation attendue.

If a non-conforming medicine is marketed outside Belgium and the medicine manufacturer is based in Belgium, the FAMHP is responsible for alerting other medicine authorities via the RAS.
If a non-conforming medicine is marketed outside Belgium and the medicine manufacturer is based in Belgium, the FAMHP is responsible for alerting other medicine authorities via the RAS.

On the basis of these European directives, the FAMHP is thus mainly responsible for supervision of the market by following up on incidents (materiovigilance) and by inspecting manufacturers, distributors and retailers established in Belgian territory.
On the basis of these European directives, the FAMHP is thus mainly responsible for supervision of the market by following up on incidents (materiovigilance) and by inspecting manufacturers, distributors and retailers established in Belgian territory.