Vertaling van "been a requirement to request " (Nederlands → Frans) :

In terms of premiums and benefits, since 1 January 2007 there has been a requirement to request a prior licence when a pharmaceutical company or company selling medical devices wishes to pay the costs of a healthcare professional participating in a scientific gathering including at least one overnight stay.
In terms of premiums and benefits, since 1 January 2007 there has been a requirement to request a prior licence when a pharmaceutical company or company selling medical devices wishes to pay the costs of a healthcare professional participating in a scientific gathering including at least one overnight stay.

Selected projects awaiting regulatory decisions Completed submissions Product Indication US EU Japan News update ABF656 Hepatitis C Q4 2009 - Dossier for ABF656 at once-everytwo-weeks dosing was withdrawn in EU in April since additional information would be requested that could not be generated within required timeframe
Projets importants en attente de décisions réglementaires Demandes déposées Produit Indication USA UE Japon Mise à jour ABF656 Hépatite C T4 2009 - Le dossier d’ABF656 comportant une dose unique toutes les 2 semaines a été retiré de l’UE en avril, car l’information supplémentaire requise ne pouvait pas être fournie dans le délai imparti

In the US, all clinical studies to support resubmission have been started following a Complete Response letter from the FDA in October 2009 requesting additional data.
Aux Etats-Unis, toutes les études cliniques destinées à soutenir le dépôt d’une nouvelle demande ont débuté après réception en octobre 2010 d’une « complete response letter » de la FDA demandant des données supplémentaires.

Since 2001, the French Agency for Food Sanitary Safety (Agence française de sécurité sanitaire des aliments, AFSSA) has been requested several times to assess the innocuousness and nutritional importance of the aforementioned drinks. It has given several negative advisory reports on this.
En effet, saisie à plusieurs reprises depuis 2001 pour évaluer l’innocuité et l’intérêt nutritionnel de la boisson déjà mentionnée ci-avant, l’Agence Française de Sécurité Sanitaire des Aliments (AFSSA) a rendu plusieurs avis négatifs.

haemovigilance data and monitoring their implementation ●● The first annual report of the Haemovigilance Centre was published in 2007 Since November 2005, hospitals and blood establishments have been required to report to the Belgian Centre for Haemovigilance of the FAMHP serious reactions during the collection or administration of blood components and serious events relating to the quality or safety of blood components.
haemovigilance data and monitoring their implementation ●● The first annual report of the Haemovigilance Centre was published in 2007 Since November 2005, hospitals and blood establishments have been required to report to the Belgian Centre for Haemovigilance of the FAMHP serious reactions during the collection or administration of blood components and serious events relating to the quality or safety of blood components.

Since 1 January 2007, the law has been in force requiring a preliminary approval for the payment by pharmaceutical companies or producers of medical devices of the participation costs of healthcare professionals in scientific events involving at least one night’s accommodation.
Since 1 January 2007, the law has been in force requiring a preliminary approval for the payment by pharmaceutical companies or producers of medical devices of the participation costs of healthcare professionals in scientific events involving at least one night’s accommodation.

Responsibility for these issues used to lie with just one inspector. Since late 2007, however, four additional employees have been active in this investigation unit, since it is clear that this area requires a specialised approach.
Responsibility for these issues used to lie with just one inspector. Since late 2007, however, four additional employees have been active in this investigation unit, since it is clear that this area requires a specialised approach.

The revised standard requires Novartis to include in the purchase consideration the estimated amount of any contingent considerations and the measurement to fair value, through the income statement of any interest in an acquired company that had been previously held.
Celle-ci requiert de Novartis d’inclure dans le prix d’acquisition le montant estimé de toute contrepartie éventuelle et d’évaluer à la juste valeur par le compte de résultat tout intérêt dans une entreprise acquise qui a été détenue précédemment.