Vertaling van "including in europe – where " (Nederlands → Frans) :

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.

In Europe, where Menveo is predominantly a travel vaccine, the first positive policy recommendations were received within a few months of approval.
En Europe, où Menveo est avant tout un vaccin de voyages, les autorités ont émis les premières recommandations favorables concernant la vaccination dans les mois qui ont suivi son homologation.

In Europe, where pricing pressures have been most intense, overall growth was 8 %, with volume gains of 12 percentage points demonstrating the quality of the new product portfolio.
En Europe, où la pression sur les prix a été la plus forte, la croissance globale s’est inscrite à 8%, avec des gains en volume de 12 points ce qui démontre la qualité des nouveaux produits.

Diovan also maintained strong growth in Europe, where the expected entry of generic versions of losartan, another medicine in the angiotensin receptor blockers (ARB) segment, has been delayed until the first half of 2010.
Diovan a également conservé une forte croissance en Europe, où l’entrée attendue de versions génériques de losartan, un autre médicament faisant partie du segment des antagonistes des récepteurs de l’angiotensine (ARA), a été repoussée au premier semestre 2010.

Japan now accounts for 20% of annual sales, while growth was seen in Europe, where the expected entry of generic versions of losartan, another medicine in the ARB segment, was delayed until the first half of 2010.
Le Japon compte maintenant pour 20% des ventes annuelles, tandis que l’Europe a progressé, l’entrée prévue de versions génériques de losartan, un autre médicament faisant partie du segment des ARA, ayant été repoussée au premier semestre 2010.

MenB, in development as a vaccine to protect against the B serogroup of meningococcal meningitis, is in Phase III studies in Europe, where patient enrollment has been completed and a regulatory submission remains on track for 2010.
MenB, en développement en tant que vaccin pour protéger contre le sérogroupe B de la méningite à méningocoque, et en études de phase II en Europe.

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.

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.

This task includes gathering information, evaluating that information and taking measures where necessary.
This task includes gathering information, evaluating that information and taking measures where necessary.