Vertaling van "authorities in countries where " (Nederlands → Frans) :

Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments.
This release contains forward-looking information that involves substantial risks and uncertainties regarding Prevenar 13, including its potential benefits; and the success of the AMC project for vaccines. Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009, and in its reports on Form 10-Q and Form 8-K.

Exelon Patch is approved for the treatment of mild to moderate Alzheimer’s disease dementia in more than 75 countries, including more than 20 countries where it is also approved for dementia associated with Parkinson’s disease.
Exelon Patch est autorisé dans plus de 75 pays pour le traitement des formes légère à modérée de la maladie d'Alzheimer et dans plus de 20 pour celui de la démence associée à la maladie de Parkinson.

Exelon Patch is approved for the treatment of mild-to-moderate Alzheimer’s disease dementia in more than 75 countries, including more than 20 countries where it is also approved for dementia associated with Parkinson’s disease.
Exelon Patch est autorisé dans plus de 75 pays pour le traitement des formes légère à modérée de la maladie d'Alzheimer et dans plus de vingt pour celui de la démence associée à la maladie de Parkinson.

Medicines discovered by the institute will be made available at cost to poor patients in those countries where they are most needed.
Les médicaments mis au point par l’Institut seront fournis à prix coûtant aux malades pauvres des pays où les besoins sont les plus urgents.

Additionally, Gilenya is currently under regulatory review in the EU, where it was filed in December 2009, and with health authorities worldwide, including Canada, Switzerland, Turkey, Brazil and Australia.
En outre, ce médicament est actuellement examiné par les autorités réglementaires de l’UE, où une demande a été déposée en novembre 2009 ainsi que par les autorités de la santé du monde entier, notamment du Canada, de la Suisse, de la Turquie, du Brésil et de l’Australie.

The Council has restricted itself to the 3 main ingredients of these drinks, viz. caffeine, taurine and D-glucuronolactone, while taking into account the opinion of the counselling authorities in the area of public health at a European level and in several countries of the European Union.
C’est donc en s’en tenant aux 3 composants principaux de ces boissons, la caféine, la taurine et le D-glucuronolactone, que le Conseil a dès lors pris en compte les avis rendus par des instances de Conseil en Santé publique au niveau européen ou dans plusieurs pays de l’Union.

It ranges from > 30% (and is still rising) in countries like the UK, France, Italy, Spain and Portugal, to less than 2% in the Netherlands and Scandinavia, where a rigid national policy is in place.
Elle s'étend à plus de 30%, et continue encore à augmenter dans des pays comme le R-U, la France, l'Italie, l'Espagne et le Portugal, à moins de 2% dans les Pays-Bas et la Scandinavie où est appliquée une politique nationale rigide.

Results of a one-year study, which was undertaken in response to “approvable letters” from the FDA, achieved primary efficacy and renal function targets and were also consistent with experience seen in 70 countries – including in Europe – where this medicine has been approved.
Les résultats d’une étude d’un an, entreprise en réponse à des «approvable letters» émises par la FDA, a atteints ses objectifs principaux en termes d’efficacité et de fonction rénale. Ces résultats étaient également en adéquation avec les expériences récoltées dans 70 pays – notamment en Europe – où ce médicament est autorisé.

Extavia (USD 26 million), for patients with relapsing forms of multiple sclerosis (MS), was first launched in the European Union in early 2009 and is now available in more than 15 countries, including the US where it was launched recently after regulatory approval was granted in August 2009.
Extavia (USD 26 millions), pour les malades atteints de formes cycliques de sclérose en plaques (SEP), a été commercialisé d’abord dans l’Union européenne début 2009.