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Acid lead arsenate
Acid lead orthoarsenate
Advanced physiotherapist
Aerial lead
Antenna down-lead
Antenna lead
Antenna lead-in
Antenna lead-in wire
Arsenate of lead
Arseniate of lead
Clinical lead
Clinical lead physiotherapist
Collect statistical data related to service delivery
Dibasic lead arsenate
Down-lead
Lead a clinical pharmacological study
Lead a clinical pharmacology study
Lead acid arsenate
Lead arsenate
Lead arseniate
Lead clinical audit
Lead clinical pharmacology studies
Lead clinical study on drug action
Lead hydrogenarsenate
Lead remedial physiotherapist
Lead-in
Non-clinical study
Pre-clinical study
Pre-clinical test
Pre-clinical testing
Pre-clinical trial
Preclinical study
Preclinical test
Preclinical trial
Senior occupational health physiotherapist
Undertake clinical audit
Undertake internal clinical audit

Traduction de «clinical lead » (Anglais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
clinical lead physiotherapist | lead remedial physiotherapist | advanced physiotherapist | senior occupational health physiotherapist

expert physiothérapeute | expert physiothérapeute/experte physiothérapeute | experte physiothérapeute




lead a clinical pharmacological study | lead clinical study on drug action | lead a clinical pharmacology study | lead clinical pharmacology studies

conduire des études pharmacologiques cliniques


collect statistical data related to service delivery | undertake internal clinical audit | lead clinical audit | undertake clinical audit

réaliser un audit clinique


A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a

déficit maternel en riboflavine


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

essai préclinique


lead hydrogenarsenate [ acid lead arsenate | acid lead orthoarsenate | arsenate of lead | arseniate of lead | dibasic lead arsenate | lead acid arsenate | lead arsenate | lead arseniate ]

hydrogénoarsénate de plomb [ hydrogénoarséniate de plomb | arsénate de plomb | arséniate de plomb ]


antenna lead-in wire [ antenna lead-in | lead-in | antenna down-lead | down-lead | antenna lead | aerial lead ]

câble de descente d'antenne [ descente d'antenne ]


A rare inflammatory eye disease of unknown aetiology characterised by generalised inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic

panuvéite idiopathique


A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive.

syndrome du grêle court congénital
TRADUCTIONS EN CONTEXTE
Only the proposal for a “clinical trials platform” for the three poverty-related diseases, which is one of the objectives of the Framework Programme, was deemed sufficiently mature, leading to further work with a view to preparing a proposal for a decision of the European Parliament and of the Council.

Seule la proposition de «plateforme d’essais cliniques» pour les trois maladies liées à la pauvreté, qui s'inscrit dans les objectifs du programme-cadre, a été jugée assez mûre et a fait l'objet de travaux subséquents en vue de préparer une proposition de décision du Parlement européen et du Conseil.


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.


Where, in the course of a clinical trial, damage caused to the subject leads to the civil or criminal liability of the investigator or the sponsor, the conditions for liability in such cases, including issues of causality and the level of damages and sanctions, should remain governed by national law.

Si, au cours d'un essai clinique, les dommages occasionnés au participant engagent la responsabilité civile ou pénale de l'investigateur ou du promoteur, les conditions de responsabilité, y compris les questions de causalité et le niveau des dommages et des sanctions, devraient, dans ce type de situation, continuer d'être régies par le droit national.


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.


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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;


Where, in the course of a clinical trial, damage caused to the subject leads to the civil or criminal liability of the investigator or the sponsor, the conditions for liability in such cases, including issues of causality and the level of damages and sanctions, should remain governed by national law.

Si, au cours d'un essai clinique, les dommages occasionnés au participant engagent la responsabilité civile ou pénale de l'investigateur ou du promoteur, les conditions de responsabilité, y compris les questions de causalité et le niveau des dommages et des sanctions, devraient, dans ce type de situation, continuer d'être régies par le droit national.


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.


Indicator: increase the number of supported clinical trials to at least 150, compared to 88 under EDCTP1, that lead to new products, processes, methodologies, diagnostics, treatments or preventions.

Indicateur: porter le nombre des essais cliniques bénéficiant d’un tel soutien à 150 au moins, contre 88 dans le cadre de l’EDCTP-I, qui permettent la mise au point de nouveaux produits, processus, méthodologies, diagnostics, traitements ou systèmes de prévention.


It is generally accepted that the Paediatric Regulation will lead to more clinical trials with children, but that its aims should be achieved without subjecting children to unnecessary clinical trials.

Il est communément admis que le règlement pédiatrique donne lieu à davantage d’essais cliniques impliquant des enfants mais que ses objectifs devraient être réalisés sans soumettre des enfants à des essais cliniques superflus.


It is generally accepted that the Paediatric Regulation will lead to more clinical trials with children, but that its aims should be achieved without subjecting children to unnecessary clinical trials.

Il est communément admis que le règlement pédiatrique donne lieu à davantage d’essais cliniques impliquant des enfants mais que ses objectifs devraient être réalisés sans soumettre des enfants à des essais cliniques superflus.


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