Vertaling van "related agreements and amendments " (Nederlands → Frans) :

On January 12, 2010, the European Commission (EC) addressed a request for information to certain pharmaceutical companies, including Novartis International AG and Sandoz International GmbH, asking them to submit copies of all of their patent settlement agreements as well as copies of all annexes, related agreements and amendments.
Le 12 janvier 2010, la Commission européenne (CE) a adressé une requête à certaines sociétés pharmaceutiques, y compris Novartis International AG et Sandoz International GmbH, leur demandant de lui fournir copie de tous leurs contrats de règlement de brevet ainsi que de toutes les annexes et de tous les accords et modifications y relatifs.

On January 12, 2010, the European Commission addressed a request for information to certain pharmaceutical companies, including Novartis International AG, asking them to submit copies of all of their patent settlement agreements as well as copies of all annexes, related agreements and amendments.
Le 12 janvier 2010, la Commission européenne a adressé une requête à certaines sociétés pharmaceutiques, y compris Novartis International AG, leur demandant de lui fournir copie de tous leurs contrats de règlement de brevet ainsi que de toutes les annexes et de tous les accords et modifications y relatifs.

In regulatory terms, the R&D department played an active part in the elaboration of the guidelines relating to substantial amendments, (N)IMP and specific arrangements for non-commercial trials.
In regulatory terms, the R&D department played an active part in the elaboration of the guidelines relating to substantial amendments, (N)IMP and specific arrangements for non-commercial trials.

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).

Pharmaceuticals – Betaseron ® On September 14, Novartis and Bayer Schering Pharma AG received regulatory approval to complete an agreement related to various rights for the multiple sclerosis treatment Betaseron ® under an earlier agreement between Schering and Chiron Corporation transferred to Novartis in April 2006.
Pharmaceuticals – Accord sur Betaseron ® lié à l’acquisition de Chiron Le 14 septembre, Novartis et Bayer Schering Pharma AG ont reçu l’autorisation des autorités de finaliser un accord portant sur différents droits du traitement contre la sclérose en plaques dénommé Betaseron ® qui avaient fait l’objet d’un accord antérieur passé entre Schering et Chiron Corporation, transféré en avril 2006 à Novartis.

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.

At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.
At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.

The operating income margin increase in the first nine months as compared to the growth in core operating income margin of 1.8 percentage points reflected the acquisition-related charges for the integration of EBEWE Pharma, one-time charges for the termination of a co-development agreement and provisions for legal settlements.
Comparée à la marge opérationnelle core qui a progressé de 1,8 point de pourcentage, la marge opérationnelle a reflété les charges d’intégration liées à l’acquisition d’EBEWE Pharma, des charges uniques pour la cessation d’un accord de codéveloppement et des provisions pour des règlements juridiques.

In September 2009, Novartis subsidiaries reached an agreement in principle 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 en vertu duquel 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.

The lower improvement of the operating margin as compared to the core operating margin increase of 1.1 percentage points reflected one-time charges related to the termination of a co-development agreement and purchase price accounting for EBEWE Pharma.
Alors que la marge opérationnelle core s’est améliorée de 1,1 point de pourcentage, l’amélioration plus faible de la marge opérationnelle est due à des charges uniques liées à la cessation d'un accord de codéveloppement et à la comptabilisation du prix d'achat d'EBEWE Pharma.