Vertaling van "role to protect the participants in clinical trials " (Nederlands → Frans) :

It is the R&D department’s role to protect the participants in clinical trials by giving scientific advice and evaluating, approving, monitoring and checking applications for clinical research, on the basis of sound scientific knowledge.
It is the R&D department’s role to protect the participants in clinical trials by giving scientific advice and evaluating, approving, monitoring and checking applications for clinical research, on the basis of sound scientific knowledge.

The safety of participants in clinical trials with investigational products (IMP) and of the users of the authorised medicines and health products is of fundamental importance.
The safety of participants in clinical trials with investigational products (IMP) and of the users of the authorised medicines and health products is of fundamental importance.

The Clinical Trial Facilitation Group (CTFG) is a collaborative effort to facilitate and harmonise clinical trials in Europe. Within the CTFG agreements have been made for various competent authorities to voluntarily arrive at a common evaluation for applications for clinical trials whenever this involves multicentre trials with participating centres from different Member States.
The Clinical Trial Facilitation Group (CTFG) is a collaborative effort to facilitate and harmonise clinical trials in Europe. Within the CTFG agreements have been made for various competent authorities to voluntarily arrive at a common evaluation for applications for clinical trials whenever this involves multicentre trials with participating centres from different Member States.

" 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

Clinical trials are underway in other age groups, including as young as from two months, to protect against the serogroups A, C, W-135 and Y found with this often-fatal bacterial infection.
Des essais cliniques sont en cours dans d’autres tranches d’âges, dès l’âge de deux mois, pour les protéger contre les sérogroupes A, C, W-135 et Y que l’on trouve dans cette maladie bactérienne souvent mortelle.

Tekturna/Rasilez (USD 119 million, +117% lc), the first new type of high blood pressure medicine in more than a decade, has accelerated its growth pace thanks to an increasing body of data affirming its ability to reduce blood pressure for more than 24 hours, its potential benefits for organ protection, and its consistent superiority in clinical trials over ramipril, a leading ACE inhibitor (another class of high blood pressure medicines).
Rasilez/Tekturna (USD 119 millions, +117% en m. l.), premier médicament d’un nouveau type contre l’hypertension depuis plus d’une décennie, a enregistré une accélération de sa croissance grâce à une masse grandissante de données faisant état de sa capacité à réduire la pression sanguine pendant plus de 24 heures, de ses bénéfices potentiels dans la protection des organes et de sa supériorité constante, manifestée lors des essais cliniques, sur le ramipril, un inhibiteur de l’IEC (une autre classe de médicaments hypotenseurs).

The R&D (research and development) department is constructed around the following three roles: ●● Clinical trials ●● GCP ●● Scientific advice
The R&D (research and development) department is constructed around the following three roles: ●● Clinical trials ●● GCP ●● Scientific advice

In zijn vergadering van 11 december 2010 besprak de Nationale Raad uw vraag van 19 mei 2010 betreffende de overdracht van materiaal afkomstig van biopsieën naar het buitenland : " Is it allowed for hospitals - the anatomo-pathological services - to send biopsy blocks of patients participating in a clinical trial and signing an informed consent, to a central laboratory outside Belgium ; e.g.
En sa séance du 11 décembre 2010, le Conseil national a examiné votre question du 19 mai 2010 concernant la transmission de prélèvements biopsiques à l'étranger : « Is it allowed for hospitals - the anatomo-pathological services - to send biopsy blocks of patients participating in a clinical trial and signing an informed consent, to a central laboratory outside Belgium ; e.g.

Clinical trials demonstrated the efficacy and safety of FTY720, with participants showing reduced relapses and delayed disease progression.
Des essais cliniques ont démontré l’efficacité et l’innocuité de FTY720 qui provoque une diminution des rechutes et un ralentissement de la progression de la maladie chez les participants.

In 2005, we participated in an industry-wide effort to improve transparency by creating an online portal, disclosing results from more than 250 000 clinical trials conducted worldwide.
En 2005, nous avons participé à une opération conjointe de tous les acteurs de notre branche en vue d’améliorer la transparence sur les essais cliniques. Un portail Internet a été créé, recensant les résultats de plus de 250’000 essais cliniques conduits à travers le monde.