Traduction de «that the clinical trial data are credible » (Néerlandais → Français) :

" Compliance with this standard (= GCP) provides public assurance that the rights, safety and well-being of trial subjects are protected, consistent with the principles that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible.‰
ÿ Compliance with this standard (= GCP) provides public assurance that the rights, safety and well-being of trial subjects are protected, consistent with the princinciples that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible. Ÿ

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.

Key drivers are clinical data demonstrating its prolonged efficacy in lowering blood pressure for more than 24 hours, and superiority in clinical trials over ramipril, a leading ACE inhibitor (an older class of high blood pressure medicines).
Les facteurs-clés de cette progression sont des données cliniques faisant état de sa capacité à réduire la pression sanguine pendant plus de 24 heures et de sa supériorité, lors d’essais cliniques, sur le ramipril, un inhibiteur important de l’IEC (une catégorie plus ancienne de médicaments hypotenseurs).

There is one other fee that is notable for its intended purpose, since the “clinical trial” contribution (1,670,042 euros) will serve not just to cover the FAMHP’s costs but also and above all to finance the Ethics Committees. As far as the taxes are concerned, it should be
There is one other fee that is notable for its intended purpose, since the “clinical trial” contribution (1,670,042 euros) will serve not just to cover the FAMHP’s costs but also and above all to finance the Ethics Committees. As far as the taxes are concerned, it should be

Data from a one-year Phase III trial published in “The New England Journal of Medicine” in June confirmed that Ilaris offered rapid and long-term clinical remission in CAPS patients.
Des données d’un essai de phase III sur un an publiées en juin dans «The New England Journal of Medicine» ont confirmé qu’Ilaris offrait une rémission clinique rapide et de longue durée des CAPS.

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.