Traduction de «which is governed under » (Néerlandais → Français) :

This merger, which is governed under the Swiss Merger Act, proposes a fixed exchange ratio of 2.80 Novartis shares for each remaining Alcon share.
Soumise à la loi fédérale suisse sur les fusions, cette fusion propose une parité fixe de 2,80 actions Novartis pour chacune des actions Alcon restantes.

Novartis believes this merger, which is governed under the Swiss Merger Act, is in the interest of all stakeholders and will provide the needed clarity on Alcon’s future.
Novartis est convaincu que cette fusion, qui sera réalisée conformément à la loi fédérale suisse sur la fusion, est dans l’intérêt de toutes les parties prenantes en apportant la clarté nécessaire à l’avenir d’Alcon.

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

Details of the agreement in principle are under discussion with relevant federal and state government offices.
Les détails de cet accord de principe sont en cours de discussion avec le bureau du procureur concerné.

Novartis ranks as having one of the industry’s most competitive pharmaceuticals development pipelines with 147 projects in clinical development, of which 27 involve new molecular entities in late-stage trials or under regulatory review.
Novartis est considéré comme possédant l’un des pipelines de produits pharmaceutiques les plus concurrentiels de l’industrie avec 147 projets en développement clinique, dont 27 impliquent de nouvelles entités moléculaires qui sont en phase ultime d’essais ou en cours d’examen par les autorités réglementaires.

Corporate – Alcon On April 7, Novartis announced an agreement with Nestlé S.A. under which Novartis obtained rights to acquire in two steps majority ownership of Alcon Inc (NYSE: ACL), a Swiss-registered company listed only on the New York Stock Exchange.
Corporate – Alcon Le 7 avril, Novartis a annoncé avoir conclu un accord avec Nestlé S.A. lui donnant le droit d’acquérir, en deux étapes, une participation majoritaire dans Alcon Inc (NYSE: ACL), une société enregistrée en Suisse mais cotée uniquement à la Bourse de New York.

Non-IFRS disclosures Net debt/liquidity and free cash flow are non-IFRS financial measures, which means they should not be interpreted as measures determined under IFRS.
Informations non-IFRS Les dettes/liquidités nettes et le free cash flow sont des grandeurs financières qui ne relèvent pas des normes IFRS, ce qui signifie qu’elles ne sauraient être interprétées comme ayant été déterminées par lesdites normes.

Export certificates Manufacturing sites under FAMHP supervision have to be able to provide documents quickly which demonstrate that the GMP conditions are being complied with.
Export certificates Manufacturing sites under FAMHP supervision have to be able to provide documents quickly which demonstrate that the GMP conditions are being complied with.

In the course of 2008 there were at least another 99 early phase trials of which 43 trials being carried out for the first time in humans, 164 phase I trials (including those not falling under the definition of an early phase trial), 176 phase II trials and 223 phase III trials. The database currently does not always allow a distinction to be made between early phase trials as defined above and later phases.
In the course of 2008 there were at least another 99 early phase trials of which 43 trials being carried out for the first time in humans, 164 phase I trials (including those not falling under the definition of an early phase trial), 176 phase II trials and 223 phase III trials. The database currently does not always allow a distinction to be made between early phase trials as defined above and later phases.

Under the terms of the CIA, which has a fixed term of five years, NPC will implement additional compliance-related measures.
Selon les termes du CIA, dont la période a été fixée à cinq ans, NPC mettra en place des mesures additionnelles de mise en conformité.