Traduction de «department of justice approval » (Néerlandais → Français) :

This agreement, which is still contingent on US Department of Justice approval, resulted in a provision of USD 38 million in the first quarter of 2010, which remains unchanged as of September 30, 2010.
Cet accord, soumis à l’approbation du Département américain de la justice, a entraîné la constitution d’une provision d’USD 38 millions au premier trimestre 2010, qui est restée inchangée au 30 septembre 2010.

In Texas, a Sandoz entity has reached an agreement in principle to settle all of the State’s claims, which is contingent upon US Department of Justice approval, resulting in a provision of USD 38 million in the first quarter of 2010.
Au Texas, une entité de Sandoz a trouvé un accord de principe pour régler toutes les plaintes de cet Etat – conditionné à l’accord du Département américain de la Justice – nécessitant de constituer une provision d'USD 38 millions au premier trimestre 2010.

In September 2009, Novartis subsidiaries reached an agreement in principle with the US Department of Justice to pay USD 72.5 million to resolve all federal and related state Medicaid claims relating to this investigation.
En septembre 2009, les filiales de Novartis sont parvenues à un accord de principe avec le Département américain de la justice selon lequel elles paieront la somme d’USD 72,5 millions pour mettre un terme à toutes les plaintes du gouvernement relatives à cette enquête.

In September 2009, Novartis subsidiaries reached an agreement in principle with the US Department of Justice to pay USD 72.5 million to resolve all federal civil claims and state Medicaid claims relating to this investigation.
En septembre 2009, les filiales de Novartis sont parvenues à un accord de principe avec le Département américain de la justice selon lequel elles paieront la somme d’USD 72,5 millions pour mettre un terme à toutes les plaintes du gouvernement et de l’Etat concernant le programme Medicaid.

Nevertheless, in view of the fact that this type of drink is already allowed in several European countries and taking into account the European regulations concerning this type of product, in the end, the competent French authorities have been obliged to give their approval (Decree of the European Court of Justice, Press release No. 12/04, 2004) for this beverage, which was marketed on 15 July 2008.
Néanmoins, considérant que ce type de boisson est déjà autorisé dans plusieurs pays d’européens et compte tenu de la réglementation européenne sur ce type de produit, les autorités compétentes françaises ont finalement dû l’autoriser (Arrêt de la Cour de Justice européenne, Communiqué de presse n° 12/04, 2004). Sa commercialisation a effectivement débuté en date du 15 juillet 2008.

The European Directive 2001/20, transposed in the law of 7 May 2004, forms the basis for the department’s core tasks: ●● Validating, evaluating and assigning approvals for the conduct of clinical trials (including declarations) ●● Strategic preparation of the associated GCP
The European Directive 2001/20, transposed in the law of 7 May 2004, forms the basis for the department’s core tasks: ●● Validating, evaluating and assigning approvals for the conduct of clinical trials (including declarations) ●● Strategic preparation of the associated GCP

It is the R&D department’s role to protect the participants in clinical trials by giving scientific advice and evaluating, approving, monitoring and checking applications for clinical research, on the basis of sound scientific knowledge.
It is the R&D department’s role to protect the participants in clinical trials by giving scientific advice and evaluating, approving, monitoring and checking applications for clinical research, on the basis of sound scientific knowledge.

The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.
The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.