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Animal trials
Apply good clinical practice
Apply good clinical practices
Apply good clinical trial practice
Assist clinical trial
Assist in clinical trials
Assisting clinical trial
Assisting clinical trials
CCT
Clinical Trial Program
Clinical Trials Program
Clinical phase
Comparative clinical trial
Comparative study
Comparative trial
Comparison study
Comparison trial
Controlled clinical study
Controlled clinical trial
Controlled study
Controlled trial
Development phases for pharmaceutical drugs
EU Database on Clinical Trials
EudraCT
European Clinical Trials Database
Meet good clinical practice standards
Multicenter clinical study
Multicenter clinical trial
Multicenter study
Multicenter trial
Multicentered clinical study
Multicentered clinical trial
Multicentered study
Multicentered trial
Multicentre clinical study
Multicentre clinical trial
Multicentre study
Multicentre trial
Non-clinical study
Pharmaceutical drug development
Pre-clinical study
Pre-clinical test
Pre-clinical testing
Pre-clinical trial
Preclinical study
Preclinical test
Preclinical trial

Traduction de «clinical trial would » (Anglais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
assist clinical trial | assisting clinical trials | assist in clinical trials | assisting clinical trial

participer à des essais cliniques


non-clinical study | preclinical study | pre-clinical study | preclinical test | pre-clinical test | pre-clinical testing | preclinical trial | pre-clinical trial

essai préclinique


multicenter trial | multicentre trial | multicenter clinical trial | multicentre clinical trial | multicentered trial | multicentered clinical trial | multicenter study | multicentre study | multicenter clinical study | multicentre clinical study | multicentered study | multicentered clinical study

essai multicentrique | essai multicentre | essai clinique multicentrique | essai clinique multicentre | étude multicentrique | étude multicentre | étude clinique multicentrique | étude clinique multicentre


comparative clinical trial | controlled clinical trial | CCT [Abbr.]

essai comparatif


EU Database on Clinical Trials | European Clinical Trials Database | EudraCT [Abbr.]

base de données de l'UE sur les essais cliniques | EudraCT [Abbr.]


apply good clinical trial practice | meet good clinical practice standards | apply good clinical practice | apply good clinical practices

appliquer la bonne pratique clinique


controlled trial | controlled clinical trial | comparative trial | comparison trial | controlled study | comparative study | comparison study | controlled clinical study

essai comparatif | essai thérapeutique comparatif | étude comparative | essai contrôlé | essai clinique contrôlé | étude contrôlée | étude clinique contrôlée


Clinical Trial Program [ Clinical Trials Program ]

Programme d'essais cliniques


controlled clinical trial | controlled trial

essai clinique contrôlé


animal trials | development phases for pharmaceutical drugs | clinical phase | pharmaceutical drug development

développement de produits pharmaceutiques
TRADUCTIONS EN CONTEXTE
Even though the certification would not be legally binding, this system should also aim at facilitating the evaluation of any future application for clinical trials and marketing authorisation application based on the same data.

Quand bien même la certification ne serait pas juridiquement contraignante, ce système devrait aussi viser à faciliter l’évaluation de toute demande ultérieure d’essais cliniques et d’autorisation de mise sur le marché reposant sur les mêmes données.


The announcement that was made in September was that there will be monitoring of the clinical trials. Those 100 patients involved in the clinical trials would be monitored.

Le gouvernement a annoncé en septembre que les essais cliniques seront surveillés, de même que les 100 patients qui y prennent part.


On Friday, the government announced that recruitment for clinical trials would begin on November 1.

Vendredi dernier, le gouvernement a annoncé que le recrutement pour les essais cliniques commencerait le 1 novembre.


when it considers that participation in the clinical trial would lead to a subject receiving an inferior treatment than in normal clinical practice in the Member State concerned.

lorsqu'il considère que la participation à l'essai clinique entraînerait pour le participant un traitement de qualité inférieure à la pratique clinique normale dans l'État membre concerné.


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As regards the second reason, the CMPHU concluded (and its assessment was not challenged by the Commission) that, because participation in a clinical trial would expose patients to the risk of serious liver damage, or even death, it would be contrary to the principles of medical ethics to carry out a controlled study of the efficacy of cholic acid.

Quant à la seconde raison, le CMHU a considéré, sans que cette appréciation soit remise en cause par la Commission, que, dans la mesure où la participation à un essai clinique exposerait les patients à un risque de lésions hépatiques graves, voire de décès, il serait contraire aux principes de déontologie médicale d’effectuer une étude contrôlée sur l’efficacité de l’acide cholique.


As regards Directive 2001/20/EC, experience also indicates that the legal form of a Regulation would present advantages for sponsors and investigators, for example in the context of clinical trials taking place in more than one Member State, since they will be able to rely on its provisions directly, but also in the context of safety reporting and labelling of investigational medicinal products.

Pour ce qui est de la directive 2001/20/CE, l'expérience montre également que la forme juridique d'un règlement présenterait des avantages pour les promoteurs et les investigateurs, notamment dans le cadre des essais cliniques conduits dans plus d'un État membre, puisqu'ils pourront invoquer directement ses dispositions, mais également dans le cadre des notifications relatives à la sécurité et de l'étiquetage des médicaments expérimentaux.


It is important for subject safety that, in addition to serious adverse events and reactions, all unexpected events that might materially influence the benefit-risk assessment of the medicinal product or that would lead to changes in the administration of a medicinal product or in overall conduct of a clinical trial are notified to the Member States concerned.

Il importe pour la sécurité des participants que, outre les événements et les effets indésirables graves, tous les événements inattendus susceptibles d'avoir une incidence importante sur l'évaluation bénéfice/risque du médicament ou d'entraîner des modifications dans l'administration du médicament ou dans la conduite générale d'un essai clinique soient notifiés aux États membres concernés.


Even though the certification would not be legally binding, this system should also aim at facilitating the evaluation of any future application for clinical trials and marketing authorisation application based on the same data.

Quand bien même la certification ne serait pas juridiquement contraignante, ce système devrait aussi viser à faciliter l’évaluation de toute demande ultérieure d’essais cliniques et d’autorisation de mise sur le marché reposant sur les mêmes données.


The issues of any material that would come from any source that goes into a clinical trial would be dealt with in the same manner that they have been answered on those questions.

Les renseignements de toutes sources mis à l'épreuve lors d'un essai clinique seront traités de la même manière que ce qui nous a été indiqué en réponse à ces questions.


Every site involved in the clinical trial would receive adverse event reports on an individual level.

Chaque site participant à un essai clinique recevait des rapports d'effets indésirables au niveau individuel.




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Date index: 2023-01-26
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