Vertaling van "under the same conditions " (Nederlands → Frans) :

Pharmaceuticals – Speedel On July 10, Novartis announced the all-cash purchase of an additional 51.7% stake in Speedel Holding AG (SIX: SPPN) through off-exchange transactions together with plans to buy all remaining shares in the Swiss biopharmaceuticals company in a mandatory public tender offer under the same conditions.
Pharmaceuticals – Speedel Le 10 juillet, Novartis a annoncé l’acquisition en espèces d’une part additionnelle de 51,7% dans Speedel Holding AG (SIX: SPPN) dans le cadre de transactions de gré à gré et son intention d’acquérir les actions restantes de cette société biopharmaceutique suisse par le biais d'une offre publique d'achat obligatoire aux mêmes conditions.

* Regardless of the case in point, your family can also be covered under the same conditions.
* Quel que soit le cas de figure, votre famille pourra également être couverte aux mêmes conditions.

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

A European regulation that has entered into force on 1 July 2004 stipulates that, in order to inform the consumer of possible health risks, the labelling of beverages that contain caffeine in a proportion in excess of 150 mg/l should contain the mention “high caffeine content” followed by the caffeine content expressed in mg/100 ml in the same field of vision as the name under which the product is sold (Directive 2002/67/EC).
Enfin, une réglementation européenne, entrée en vigueur au 1er juillet 2004, stipule que l’étiquetage de boissons contenant plus de 150 mg de caféine par litre doit comporter la mention « teneur élevée en caféine » et la mention de sa quantité (en mg/100 ml) dans le même champ de vision du produit afin d’avertir le consommateur des risques possibles pour la santé (Directive 2002/67/CE).

Two clinical studies recently confirmed rapid and sustained improvement in vision with Lucentis in another debilitating eye condition, visual impairment due to diabetic macular edema (DME), currently under regulatory review in the EU.
Deux études cliniques récentes ont confirmé que Lucentis améliorait rapidement et durablement la vision dans une autre affection invalidante de l'œil due à l’œdème maculaire diabétique.

Consumer Health: USD 5.8 billion (+0%, +5% lc) All businesses achieved faster underlying growth than their respective markets despite the difficult economic conditions.
Consumer Health: USD 5,8 milliards (+0%, +5% en m. l).

Hirai Y. Survival of bacteria under dry conditions; from a viewpoint of nosocomial infection.
- Hirai Y. Survival of bacteria under dry conditions; from a viewpoint of nosocomial infection.

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.