Vertaling van "clinical trial activities " (Nederlands → Frans) :

R&D increased 0.3 percentage points, mainly driven by phasing of clinical trial activities.
Recherche et développement s’est amélioré de 0,3 point, essentiellement à la suite d’un étalement des essais cliniques dans le temps.

R&D improved 0.3 percentage points, mainly driven by phasing of clinical trial activities.
La R&D s’est améliorée de 0,3 point, essentiellement à la suite d’un étalement dans le temps des essais cliniques.

R&D improved 0.7 percentage points, mainly driven by phasing of clinical trial activities.
La R&D s’est améliorée de 0,7 point de pourcentage, essentiellement à la suite d’un étalement dans le temps des essais cliniques.

However, the figures do clearly show that there is a considerable number of early phase trials. There are 7 units in Belgium actively undertaking phase I clinical trials and a number of early phase trials are being conducted in centres where there is expertise in specific clinical areas.
However, the figures do clearly show that there is a considerable number of early phase trials. There are 7 units in Belgium actively undertaking phase I clinical trials and a number of early phase trials are being conducted in centres where there is expertise in specific clinical areas.

The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.
The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.

The FAMHP intends to significantly increase its involvement in the lifecycle of immunological medicines for veterinary use by providing scientific advice, evaluating applications for clinical trials in Belgium, adopting (co-)rapporteurships for CP, MRP and DCP for MA of vaccines for veterinary use and developing pharmacovigilance and inspection activities.
The FAMHP intends to significantly increase its involvement in the lifecycle of immunological medicines for veterinary use by providing scientific advice, evaluating applications for clinical trials in Belgium, adopting (co-)rapporteurships for CP, MRP and DCP for MA of vaccines for veterinary use and developing pharmacovigilance and inspection activities.