Traduction de «products issued » (Néerlandais → Français) :

TERMINOLOGIE

product dat aescine bevat
produit contenant de l'aescine

product dat balsalazide bevat
produit contenant du balsalazide

product dat bacitracine bevat
produit contenant de la bacitracine

product dat basiliximab bevat
produit contenant du basiliximab

product dat baclofen bevat
produit contenant du baclofène

product dat auranofine bevat
produit contenant de l'auranofine

product dat auranofine in orale vorm bevat
produit contenant de l'auranofine sous forme orale

product dat enkel auranofine in orale vorm bevat
produit contenant seulement de l'auranofine sous forme orale

product dat barbituraat bevat
produit contenant du barbiturique

product dat baricitinib bevat
produit contenant du baricitinib

TRADUCTIONS EN CONTEXTE

Herbal medicinal products In line with the provisions of the royal decree of 14 December 2006, three procedures are used for the issue of the MA or registration for herbal medicinal products: the full procedure, the “Well Established Use” procedure and a third specific procedure for traditional herbal medicines as stipulated in article 43 of the royal decree.
Herbal medicinal products In line with the provisions of the royal decree of 14 December 2006, three procedures are used for the issue of the MA or registration for herbal medicinal products: the full procedure, the “Well Established Use” procedure and a third specific procedure for traditional herbal medicines as stipulated in article 43 of the royal decree.

European Union regulatory approval is anticipated soon, after the Committee for Medicinal Products (CHMP) issued a positive opinion in May supporting approval in renal cell carcinoma following progression on VEGF-targeted therapy.
Dans l’Union européenne, l’autorisation est attendue sous peu dès lors que le Committee for Medicinal Products (CHMP) a émis un avis favorable soutenant l’homologation dans le carcinome des cellules rénales à la suite de la progression du traitement ciblé sur le VEGF.

Courts in the Netherlands (February 2009) and France (March 2009) issued rulings holding that CIBA Vision’s patents were valid and infringed by J&J’s sales of Oasys ® products.
Aux Pays-Bas (février 2009) et en France (mars 2009), les tribunaux ont conclu que les brevets de CIBA Vision étaient valables et violés par les ventes des produits Oasys ® de J&J.

Courts in the Netherlands (February 2009), France (March 2009) and the US (August 2009) issued rulings holding that CIBA Vision’s patents were valid and infringed by J&J’s sales of Oasys ® products.
Aux Pays-Bas (février 2009), en France (mars 2009) et aux Etats-Unis (août 2009), les tribunaux ont conclu que les brevets de CIBA Vision étaient valables et violés par les ventes des produits Oasys ® de J&J.

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.

The increased productivity is the result of concrete measures within the Registration department and has ensured that more MA are issued for medicines.
The increased productivity is the result of concrete measures within the Registration department and has ensured that more MA are issued for medicines.

●● Efficacy: the active ingredient is as such subject to an authorisation or prequalification by the WHO or a positive opinion from the EMEA During this first year of activity, The Production & Distribution department issued 149 EDs.
●● Efficacy: the active ingredient is as such subject to an authorisation or prequalification by the WHO or a positive opinion from the EMEA During this first year of activity, The Production & Distribution department issued 149 EDs.