Traduction de «points and provisions for settlement » (Néerlandais → Français) :

Key factors for the reduction included acquisitionrelated charges for the EBEWE Pharma integration (–0.7 percentage points), exceptional costs for termination of a co-development agreement (–0.8 percentage points) and provisions for settlement of Average Wholesale Pricing litigation in the US (–1.9 percentage points).
Les principaux facteurs de cette réduction sont des charges liées à l’intégration d’EBEWE Pharma (–0,7 point de pourcentage), des coûts exceptionnels pour la cessation d’un accord de codéveloppement (–0.8 point) et des provisions pour le règlement du litige concernant le prix de gros moyen aux Etats-Unis (–1.9 point).

Exceptional items: Other income includes mainly a Swiss pension curtailment gain of USD 265 million in Corporate, proceeds of USD 42 million from a legal settlement in Pharmaceuticals with Teva regarding Famvir and a divestment gain of USD 33 million for Tofranil in Pharmaceuticals; Other expense includes a USD 152.5 million provision for a gender discrimination case in the US in Pharmaceuticals, a USD 26 million charge for restructuring in the US in Pharmaceuticals, a USD 25.5 million provision in connection with a government investigation in the US in Pharmaceuticals, a USD 45 million charge for a legal settlement in Vaccines and Diagnostics, and a USD 38 million charge for a legal settlement in Sandoz; Income from associated companies reflects an additional charge of USD 43 million for the Novartis share of Roche’s restructuring charges for Genentech taken in the second half of 2009.
Autres produits comprend principalement un gain lié à des modifications de la comptabilisation de régimes de retraites d’USD 265 millions dans Corporate, un produit d’USD 42 millions provenant d’un règlement juridique avec Teva concernant Famvir et un gain de cession d’USD 33 millions pour Tofranil; Autres charges comprend USD 152,5 millions pour le règlement provisoire d’un cas de discrimination sexuelle aux USA, une charge de restructuration d’USD 26 millions aux ESA dans Pharmaceuticals, une provision d’USD 25,5 millions liée à une enquête gouvernementale aux USA dans Pharmaceuticals, une charge d’USD 45 millions pour un règlement juridique dans Vaccins et Diagnostic et une charge d’USD 38 millions pour un règlement juridique dans Sandoz ; Quote-part du résultat net des entreprises associées reflète une charge supplémentaire d’USD 43 millions pour la part de Novartis dans les frais de restructuration de Genentech supportés par Roche enregistrés au second semestre 2009.

Exceptional items: Other income includes mainly a Swiss pension curtailment gain of USD 265 million in Corporate, proceeds of USD 42 million from a legal settlement in Pharmaceuticals with Teva regarding Famvir and a divestment gain of USD 33 million for Tofranil in Pharmaceuticals; Other expense includes mainly a USD 152.5 million provision for a gender discrimination case in the US in Pharmaceuticals, a USD 26 million charge for restructuring in the US in Pharmaceuticals, a USD 25.5 million provision in connection with a government investigation in the US in Pharmaceuticals, USD 45 million for a legal settlement in Vaccines and Diagnostics, and a USD 38 million charge for a legal settlement in Sandoz; Income from associated companies reflects an additional charge of USD 43 million for the Novartis share of Roche’s restructuring charges for Genentech taken in the second half of 2009.
Eléments exceptionnels: Autres produits comprend principalement un gain d’USD 265 millions dans Corporate provenant du changement du régime des retraites en Suisse, des produits d’USD 42 millions dans Pharmaceuticals provenant d’un réglement juridique avec Teva concernant Famvir et un gain d’USD 33 millions dans Pharmaceuticals provanant de la cession de Tofranil; Autres charges comprend principalement une provision d’USD 152,5 millions dans Pharmaceuticals pour un cas de discrimination sexuelle aux USA, une charge d’USD 26 million pour la restructuration de Pharmaceuticals aux USA, une provision d’USD 25,5 millions dans Pharmaceutical en lien avec une enquête gouvernementale aux USA, un montant d’USD 45 millions dans Vaccins et Diagnostique pour un règlement juridique et une charge d’USD 38 millions dans Sandoz pour un règlement juridique; Quote-part dans le résultat des entreprises associées reflète une charge supplémentaire d’USD 43 millions concernant des charges de restructuration de Roche pour Genentech au second semestre 2009.

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.

Exceptional items: Other income reflects proceeds of USD 42 million from a legal settlement with Teva regarding Famvir and a divestment gain of USD 33 million for Tofranil; Other expense includes a USD 152.5 million provision for a gender discrimination case in the US, a USD 26 million charge for restructuring in the US as well as a USD 25.5 million provision in connection with a government investigation in the US.
Eléments exceptionnels: Autres produits comprend un produit d’USD 42 millions provennat d’un règlement juridique avec Teva concernant Famvir et un gain de cession d’USD 33 millions pour Tofranil; Autres charges comprend une provision d’USD 152,5 millions pour un cas de discrimination sexuelle aux USA, une charge de restructuration d’USD 26 millions aux USA ainsi qu’une provision d’USD 25,5 millions en lien avec une enquête gouvernementale aux USA.

Exceptional items: R&D includes an expense for termination of a co-development contract; Other income includes mainly a Swiss pension curtailment gain of USD 265 million in Corporate and a divestment gain of USD 33 million for Tofranil in Pharmaceuticals; Other expense includes a USD 152.5 million provision for a gender discrimination case in the US in Pharmaceuticals, USD 45 million for a legal settlement in Vaccines and Diagnostics, a USD 26 million charge for restructuring in the US in Pharmaceuticals as well as a USD 25.5 million provision in connection with a government investigation in the US in Pharmaceuticals.
Eléments exceptionnels: Recherche et développement comprend une charge pour la cessation d’un contrat de codéveloppement; Autres produits comprend principalement un gain lié à des modifications de la comptabilisation de régimes de retraites d’USD 265 millions et un gain de cession d’USD 33 millions pour Tofranil dans Pharmaceuticals; Autres charges comprend USD 152,5 millions pour le règlement provisoire d’un cas de discrimination sexuelle aux USA dans Pharmaceuticals, USD 45 millions pour un règlement juridique dans Vaccins et Diagnostic, une charge de restructuration d’USD 26 millions aux USA dans Pharmaceuticals ainsi qu’une provision d’USD 25,5 millions liée à une enquêtre gouvernementale aux USA dans Pharmaceuticals.

The total overall settlement amount of USD 422.5 million was fully provisioned for as of the end of the second quarter of 2010.
Le montant total du règlement qui s’élève à USD 422,5 millions a été intégralement provisionné à la fin du deuxième trimestre 2010.

1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines
1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines

In close cooperation with Mdeon, the FAMHP has mainly focused on the provision of information to the relevant parties, i.e. companies and healthcare professionals, during this first operational year A “contact point” collects and processes information about actions that may constitute an infringement of the legal requirements about advertising. In terms of advertising for healthcare professionals, attention is particularly being focused at present on the conformity of the legally required information
In close cooperation with Mdeon, the FAMHP has mainly focused on the provision of information to the relevant parties, i.e. companies and healthcare professionals, during this first operational year A “contact point” collects and processes information about actions that may constitute an infringement of the legal requirements about advertising. In terms of advertising for healthcare professionals, attention is particularly being focused at present on the conformity of the legally required information

On the other hand, the federal Minister of Public Health points out that, until harmonised provisions have been introduced at the European level, caffeine falls under the food additives legislation in Belgium and that this harmonisation will be carried out in a different context than the food additives legislation.
Par ailleurs, le Ministre Fédéral de la Santé Publique précise clairement que la caféine relève en Belgique de la législation sur les additifs jusqu’à ce qu’une harmonisation soit opérée à l’échelon européen et que cette harmonisation se fera dans un autre cadre que celui de la législation sur les additifs.