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Applicator voor aneurysmaclip
Applicator voor compressiekousen
Applicator voor dermale anesthesie
Applicator voor tandheelkundige hars
Applicator voor thermisch pulsatiesysteem voor ooglid

Vertaling van "evaluation of applications " (Nederlands → Frans) :

TERMINOLOGIE
extracorporele applicator voor hyperthermiesysteem voor extravasculaire circulatie

applicateur extracorporel de système d’hyperthermie de circulation extravasculaire








handbediende applicator voor brachytherapiesysteem voor oog

applicateur manuel de système de brachythérapie oculaire


applicator voor thermisch pulsatiesysteem voor ooglid

applicateur pour système de traitement thermique par impulsions sur les paupières


intracorporele applicator voor hyperthermiesysteem voor extravasculaire circulatie

applicateur intracorporel de système d’hyperthermie de circulation extravasculaire


handbediende applicator voor oesofageaal brachytherapiesysteem

applicateur manuel de système de brachythérapie pour l’œsophage


applicator voor oesofageaal brachytherapiesysteem met op afstand bedienbare afterloading

applicateur de système de brachythérapie pour l’œsophage à chargement différé à distance


IN-CONTEXT TRANSLATIONS
Considérant que l’article 144, § 1er, de la loi relative à l’assurance obligatoire soins de santé et indemnités, coordonnée le 14 juillet 1994, énonce que les chambres de recours instituées auprès du Service d’évaluation et de contrôle médicaux de l’INAMI sont des juridictions administratives; que ni cette loi ni l’arrêté royal du 9 mai 2008 fixant les règles de fonctionnement et le règlement de procédure des chambres de première instance et des chambres de recours instituées auprès du Service d’évaluation et de contrôle médicaux de ...[+++]

Considérant que l'article 144, § 1 er , de la loi relative à l'assurance obligatoire soins de santé et indemnités, coordonnée le 14 juillet 1994, énonce que les chambres de recours instituées auprès du Service d'évaluation et de contrôle médicaux de l'INAMI sont des juridictions administratives; que ni cette loi ni l'arrêté royal du 9 mai 2008 fixant les règles de fonctionnement et le règlement de procédure des chambres de première instance et des chambres de recours instituées auprès du Service d'évaluation et de contrôle médicaux d ...[+++]


Considerable attention was focused in 2007 on increased cooperation on the part of the FAMHP with the ethics committees, with the following results: ●● An interactive website with a web application that makes possible the “simple” management of communication actions between the different ethics committees, the FAMHP, the sponsors and researchers, and also monitors the different stages in the evaluation of each application by the ethics committees ●● Systematic consultation for the more complex scientific applications ●● Further optimisa ...[+++]

Considerable attention was focused in 2007 on increased cooperation on the part of the FAMHP with the ethics committees, with the following results: ●● An interactive website with a web application that makes possible the “simple” management of communication actions between the different ethics committees, the FAMHP, the sponsors and researchers, and also monitors the different stages in the evaluation of each application by the ethics committees ●● Systematic consultation for the more complex scientific applications ●● Further optimisa ...[+++]


Some achievements of the evaluation commission for herbal medicines (plants working group) in 2007 were ●● The monitoring of applications ●● The first applications for TU registration ●● The TU notification project ●● Interaction with the “grey area” consultation

Some achievements of the evaluation commission for herbal medicines (plants working group) in 2007 were ●● The monitoring of applications ●● The first applications for TU registration ●● The TU notification project ●● Interaction with the “grey area” consultation


The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.

The Registration (marketing authorisation) department of the FAMHP is responsible for evaluating new applications and applications for changes to existing marketing authorisations (variations), with a view to grant the authorisation for marketing a medicine or health product.


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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.


U.S. Food and Drug Administration – Center for drug evaluation and research “Application number 21-395.

U.S. Food and Drug Administration – Center for drug evaluation and research”Application number 21-395.


The Belgian delegation is attempting to play an important role in this process by putting its name forward as candidate for evaluating vaccine applications.

The Belgian delegation is attempting to play an important role in this process by putting its name forward as candidate for evaluating vaccine applications.


This agreement provides for an enhanced collaboration between the two institutions in the evaluation of quality data in applications for MA or associated amendments (variations) for vaccines for veterinary use, “Good Manufacturing Practices” inspection (GMP) and post-marketing reviews (monitoring by the FAMHP on samples taken).

This agreement provides for an enhanced collaboration between the two institutions in the evaluation of quality data in applications for MA or associated amendments (variations) for vaccines for veterinary use, “Good Manufacturing Practices” inspection (GMP) and post-marketing reviews (monitoring by the FAMHP on samples taken).


Les objectifs de ce rapport sont : d’une part, d’étudier comment concevoir un système d’évaluation de la performance du système de soins de santé d’autre part, d’examiner son application possible en Belgique en construisant et en mesurant un premier ensemble d’indicateurs.

De doelstellingen van dit rapport: enerzijds nagaan hoe een systeem voor de evaluatie van de performantie van het gezondheidssysteem kan worden uitgewerkt anderzijds de mogelijke toepassing ervan in België onderzoeken door een eerste reeks indicatoren samen te stellen en te bepalen.


Encouraging clinical trials and the inherent evaluation of applications for these trials, as well as the creation of a scientific subgroup for oncology, means that the FAMHP will need to have the necessary autonomy to attract the essential expertise for this relatively complex domain from the point of concept of innovative medicines.

Encouraging clinical trials and the inherent evaluation of applications for these trials, as well as the creation of a scientific subgroup for oncology, means that the FAMHP will need to have the necessary autonomy to attract the essential expertise for this relatively complex domain from the point of concept of innovative medicines.




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Date index: 2022-11-20
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