Vertaling van "following eu approval in december " (Nederlands → Frans) :

Onbrez Breezhaler (QAB149, indacaterol) (USD 8 million) has demonstrated promising performance following EU approval in December 2009 as a once-daily long-acting beta-2 agonist (LABA) for adults with chronic obstructive pulmonary disease (COPD).
Onbrez Breezhaler (QAB149, indacaterol) (USD 8 millions) a enregistré une performance prometteuse après son homologation en décembre 2009 par l’UE en tant qu’antagoniste beta 2 à action prolongée en prise unique quotidienne pour les adultes souffrant de broncho-pneumopathie chronique obstructive (BPCO).

QAB149 (indacaterol) was submitted for US and EU approvals in December 2008 as a 24-hour bronchodilator for chronic obstructive pulmonary disease (COPD), an incurable condition in which the lungs have been damaged, usually from smoking.
QAB149 (indacatérol) a fait l’objet du dépôt d’une demande d’enregistrement aux Etats- Unis et en Europe en tant que broncho-dilatateur efficace durant 24 heures contre la broncho-pneumopathie chronique obstructive (BPCO), une maladie incurable qui conduit à une altération des poumons, causée habituellement par la fumée.

Tasigna (USD 212 million, +145% lc), a second-line therapy for patients with a form of chronic myeloid leukemia (CML) resistant or intolerant to prior therapy, including Gleevec/Glivec, has gained rapid acceptance following its approval in more than 80 countries.
Tasigna (USD 212 millions, +145% en m. l.), traitement de deuxième intention pour les malades atteints d’une forme de leucémie myéloïde chronique (LMC) présentant une résistance ou une intolérance aux traitements antérieurs, Glivec/Gleevec inclus, est rapidement accepté depuis que plus de 80 pays l'ont autorisé.

Onbrez Breezhaler (USD 5 million) has demonstrated strong performance following EU approval and since first launching in late 2009 in Germany for adult patients with chronic obstructive pulmonary disease (COPD).
Onbrez Breezhaler (USD 5 millions) a réalisé une excellente performance à la suite de son homologation dans l’UE et depuis son premier lancement à fin 2009 en Allemagne pour le traitement des adultes souffrant de broncho-pneumopathie chronique obstructive (BPCO).

Under the new agreement, Novartis received a one-time payment of USD 200 million, principally for manufacturing facilities transferred to Bayer Schering, as well as receiving rights to market a Novartis-branded version of Betaseron ® called Extavia starting in 2009 in the EU and later in the US following anticipated approval.
En vertu de ce nouvel accord, Novartis a reçu un paiement unique d’USD 200 millions, principalement pour le transfert de sites de production à Bayer Schering ainsi que les droits de commercialisation sous la marque Novartis d’une version Betaseron ® appelée Extavia débutant en 2009 en Europe et plus tard au cours de l’année aux Etats-Unis à la suite de l’autorisation attendue.

Glivec received European regulatory approval in May 2009 as a post-surgery (adjuvant setting) therapy for GIST following Swiss (February 2009) and US (December 2008) approvals.
Glivec a été homologué en mai 2009 par les autorités européennes comme traitement adjuvant postchirurgical contre les GIST, à la suite de la Suisse (février 2009) et des Etats-Unis (décembre 2008).

EU approval was received for Diovan in treating pediatric hypertension, following a positive CHMP opinion in December 2009.
L’homologation de Diovan par l’Union européenne (UE) pour le traitement de l’hypertension pédiatrique, à la suite d’un avis favorable du CHMP émis en décembre 2009.

On 23 December 2005, approval was granted by the Council of Ministers for the establishment of an autonomous medicines agency: the Federal Agency for Medicines and Health Products or FAMHP.
On 23 December 2005, approval was granted by the Council of Ministers for the establishment of an autonomous medicines agency: the Federal Agency for Medicines and Health Products or FAMHP.

Following a brief review of the legislation regarding the establishment of the Scientific Committee and the selection of the president, the members approved the rules and regulations.
Following a brief review of the legislation regarding the establishment of the Scientific Committee and the selection of the president, the members approved the rules and regulations.

In 2007, the organisation’s own income included an exceptional contribution of 4,793,620 euros allocated in connection with the formation of the FAMHP by articles 241 and following of the programme law of 27 December 2006.
In 2007, the organisation’s own income included an exceptional contribution of 4,793,620 euros allocated in connection with the formation of the FAMHP by articles 241 and following of the programme law of 27 December 2006.