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1 kilometre time trial
1000m time trial
1km time trial
Arrest pending trial
Assist clinical trial
Assist in clinical trials
Assisting clinical trial
Assisting clinical trials
Bike trial
Bike trials
Calculate trial accounting balances
Collaborative study
Collaborative trial
Detention on remand
Detention pending trial
Formulate trial accounting balances
Get involved in the day-to-day operations
Interlaboratory study
Interlaboratory trial
Kilometer time trial
Kilometre time trial
Make trial accounting balances ready
Multi-centre clinical trial
Multi-centre study
Multi-centre trial
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-blinded study
Non-blinded trial
Nonblinded study
Nonblinded trial
Open study
Open trial
Open-label study
Open-label trial
Pre-trial detention
Prepare trial accounting balances
Provisional custody
Provisional detention
Remand in custody
Remand in custody pending trial
Ring trial
Take part in the day-to-day operation of the company
Trial
Trials
Unblinded study
Unblinded trial

Traduction de «trials involving » (Anglais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
arrest pending trial | detention on remand | detention pending trial | pre-trial detention | provisional custody | provisional detention | remand in custody | remand in custody pending trial

détention avant jugement | détention préventive | détention provisoire


assist clinical trial | assisting clinical trials | assist in clinical trials | assisting clinical trial

participer à des essais cliniques


formulate trial accounting balances | make trial accounting balances ready | calculate trial accounting balances | prepare trial accounting balances

préparer des balances de comptes


getting involved in the day-to-day operation of the company | take part in the day-to-day operation of the company | get involved in the day-to-day operation of the company | get involved in the day-to-day operations

s’impliquer dans les activités quotidiennes de l’entreprise


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


open trial | open-label trial | unblinded trial | nonblinded trial | non-blinded trial | open study | open-label study | unblinded study | nonblinded study | non-blinded study

essai ouvert | essai non aveugle | essai libre | essai avec étiquetage en clair | essai sans insu | essai non à l'insu | essai en mode libre | étude ouverte | étude non aveugle | étude non à l'insu | étude en mode libre


kilometre time trial [ kilometer time trial | 1 kilometre time trial | 1km time trial | 1000m time trial ]

1 kilomètre contre la montre [ kilomètre contre la montre | km contre la montre | kilomètre départ arrêté ]


multicenter study | multicenter trial | multi-centre clinical trial | multi-centre study | multi-centre trial

essai clinique multicentrique


collaborative study | collaborative trial | interlaboratory study | interlaboratory trial | ring trial

analyse interlaboratoire | essai circulaire | étude collaborative


TRADUCTIONS EN CONTEXTE
2. In the case of a clinical trial involving the use of more than one investigational medicinal product, the sponsor may, if provided for in the protocol, submit a single safety report on all investigational medicinal products used in that clinical trial.

2. Si l'essai clinique implique l'utilisation de plusieurs médicaments expérimentaux, le promoteur peut, si le protocole le prévoit, transmettre un seul rapport sur la sécurité pour tous les médicaments expérimentaux utilisés au cours de cet essai clinique.


Specific expertise should be considered when assessing clinical trials involving subjects in emergency situations, minors, incapacitated subjects, pregnant and breastfeeding women and, where appropriate, other identified specific population groups, such as elderly people or people suffering from rare and ultra rare diseases.

Il convient, lors de l'évaluation d'essais cliniques portant sur des participants en situation d'urgence, des mineurs, des participants incapables, des femmes enceintes ou allaitantes et, le cas échéant, sur d'autres catégories de populations spécifiques identifiées, telles que les personnes âgées ou les patients atteints de maladies rares ou ultra-rares, de s'appuyer sur une expertise spécifique.


If only one Member State concerned is willing to be the reporting Member State or if the clinical trial involves only one Member State, that Member State shall be the reporting Member State.

Si un seul État membre concerné est disposé à devenir rapporteur ou si l'essai clinique ne fait intervenir qu'un seul État membre, cet État membre devient rapporteur.


5. For clinical trials involving more than one Member State, the assessment process shall include three phases:

5. Pour les essais cliniques faisant intervenir plus d'un État membre, le processus d'évaluation comprend trois phases:


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Specific expertise must be used to assess clinical trials involving participants in emergency situations, minors, those who are incapacitated, pregnant and breast-feeding women and, where appropriate, certain other groups, such as older people or those suffering from rare and extremely rare diseases.

Des compétences spécifiques doivent être utilisées pour évaluer les essais cliniques impliquant des participants en situation d’urgence, des mineurs, des personnes invalides, des femmes enceintes ou allaitantes ou, le cas échéant, certains autres groupes dont font partie les personnes âgées ou les personnes souffrant d’une maladie rare ou extrêmement rare.


2. In the case of a clinical trial involving the use of more than one investigational medicinal product, the sponsor may, if provided for in the protocol, submit a single safety report on all investigational medicinal products used in that clinical trial.

2. Si l'essai clinique implique l'utilisation de plusieurs médicaments expérimentaux, le promoteur peut, si le protocole le prévoit, transmettre un seul rapport sur la sécurité pour tous les médicaments expérimentaux utilisés au cours de cet essai clinique.


Specific expertise should be considered when assessing clinical trials involving subjects in emergency situations, minors, incapacitated subjects, pregnant and breastfeeding women and, where appropriate, other identified specific population groups, such as elderly people or people suffering from rare and ultra rare diseases.

Il convient, lors de l'évaluation d'essais cliniques portant sur des participants en situation d'urgence, des mineurs, des participants incapables, des femmes enceintes ou allaitantes et, le cas échéant, sur d'autres catégories de populations spécifiques identifiées, telles que les personnes âgées ou les patients atteints de maladies rares ou ultra-rares, de s'appuyer sur une expertise spécifique.


7. The reporting Member State may also extend the period referred to in paragraph 4 by a further 50 days for clinical trials involving an advanced therapy investigational medicinal products or a medicinal product as defined in point 1 of the Annex to Regulation (EC) No 726/2004, for the purpose of consulting with experts.

7. L'État membre rapporteur peut également prolonger le délai visé au paragraphe 4 de cinquante jours supplémentaires pour des essais cliniques faisant intervenir un médicament expérimental de thérapie innovante ou des médicaments au sens du point 1 de l'annexe du règlement (CE) no 726/2004, afin de permettre la consultation d'experts.


If only one Member State concerned is willing to be the reporting Member State or if the clinical trial involves only one Member State, that Member State shall be the reporting Member State.

Si un seul État membre concerné est disposé à devenir rapporteur ou si l'essai clinique ne fait intervenir qu'un seul État membre, cet État membre devient rapporteur.


5. For clinical trials involving more than one Member State, the assessment process shall include three phases:

5. Pour les essais cliniques faisant intervenir plus d'un État membre, le processus d'évaluation comprend trois phases:




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Date index: 2022-03-20
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