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1 kilometre time trial
1000m time trial
1km time trial
Arrest pending trial
Bike trial
Bike trials
Collaborative study
Collaborative trial
Detention on remand
Detention pending trial
Determine creatively about jewellery
Educate staff about product features
Examine complaints about improper waste handling
Explore complaints about improper waste handling
Follow up on complaints about improper waste handling
Interlaboratory study
Interlaboratory trial
Investigate complaints about improper waste handling
Kilometer time trial
Kilometre time trial
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
Provisional custody
Provisional detention
Remand in custody
Remand in custody pending trial
Ring trial
Surmise creatively about jewellery
Teach staff about product features
Think creatively about jewellery
Thinking creatively about jewellery
Train staff about product features
Training staff about a product feature
Trial
Trials
Unblinded study
Unblinded trial

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

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
examine complaints about improper waste handling | explore complaints about improper waste handling | follow up on complaints about improper waste handling | investigate complaints about improper waste handling

examiner des plaintes concernant une mauvaise gestion des déchets


surmise creatively about jewellery | thinking creatively about jewellery | determine creatively about jewellery | think creatively about jewellery

faire preuve de créativité dans la fabrication de bijoux


educate staff about product features | teach staff about product features | train staff about product features | training staff about a product feature

former le personnel sur les caractéristiques de produits


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


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 ]


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

analyse interlaboratoire | essai circulaire | étude collaborative


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

essai clinique multicentrique


TRADUCTIONS EN CONTEXTE
5. Informed consent: prior to the trial, participants must be given clear information about their rights (including the right to withdraw); conditions, duration, nature, objectives, implications, risks and inconveniences of the trial; possible treatment alternatives; and the possible damage compensation system.

Consentement éclairé: avant l’essai, les participants doivent recevoir des informations claires sur leurs droits (y compris le droit de se retirer), les conditions, la durée, la nature, les objectifs, les implications, les risques et les inconvénients de l’essai, d’éventuels traitements alternatifs et d’éventuelles indemnités en cas de dommages.


General information about the clinical trial (including information about main objectives of the trial, trial design, scientific background and explanation of rationale for the trial; date of the start of the trial, measures of protection of subjects taken, background therapy; and statistical methods used).

Informations générales relatives à l'essai clinique (y compris des informations sur les objectifs principaux de l'essai, la conception de l'essai, le contexte scientifique et l'explication de la logique de l'essai; la date de début de l'essai, les mesures prises pour la protection des participants, le traitement de base, et les méthodes statistiques employées).


General information about the clinical trial (including where and when the trial was conducted, the main objectives of the trial and an explanation of the reasons for conducting it).

informations générales relatives à l'essai clinique (y compris le lieu et la date de réalisation de l'essai, les objectifs principaux de l'essai et une explication des raisons pour lesquelles l'essai est mené).


5. Informed consent: prior to the trial, participants must be given clear information about their rights (including the right to withdraw); conditions, duration, nature, objectives, implications, risks and inconveniences of the trial; possible treatment alternatives; and the possible damage compensation system.

Consentement éclairé: avant l’essai, les participants doivent recevoir des informations claires sur leurs droits (y compris le droit de se retirer), les conditions, la durée, la nature, les objectifs, les implications, les risques et les inconvénients de l’essai, d’éventuels traitements alternatifs et d’éventuelles indemnités en cas de dommages.


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include the EU trial number and information about the availability of the clinical trial results in accordance with paragraph 6.

comprennent le numéro UE d'essai ainsi que des informations sur la disponibilité des résultats de l'essai clinique conformément au paragraphe 6.


General information about the clinical trial (including information about main objectives of the trial, trial design, scientific background and explanation of rationale for the trial; date of the start of the trial, measures of protection of subjects taken, background therapy; and statistical methods used);

Informations générales relatives à l'essai clinique (y compris des informations sur les objectifs principaux de l'essai, la conception de l'essai, le contexte scientifique et l'explication de la logique de l'essai; la date de début de l'essai, les mesures prises pour la protection des participants, le traitement de base, et les méthodes statistiques employées).


General information about the clinical trial (including where and when the trial was conducted, the main objectives of the trial and an explanation of the reasons for conducting it);

informations générales relatives à l'essai clinique (y compris le lieu et la date de réalisation de l'essai, les objectifs principaux de l'essai et une explication des raisons pour lesquelles l'essai est mené);


include the EU trial number and information about the availability of the clinical trial results in accordance with paragraph 6.

comprennent le numéro UE d'essai ainsi que des informations sur la disponibilité des résultats de l'essai clinique conformément au paragraphe 6.


First, clinical trials remain the main means to obtain reliable information about the efficacy and safety profile of a medicinal product and the systematic administration of complex medicinal products to patients in the absence of appropriate clinical trials could put patients at risk.

Premièrement, les essais cliniques restent le principal moyen de recueillir des informations fiables sur le profil d’efficacité et de sécurité d’un médicament, et l’administration systématique de médicaments complexes en l’absence d’essais cliniques appropriés pourrait mettre les patients en danger.


5. Informed consent: prior to the trial, participants must be given clear information about their rights (including the right to withdraw); conditions, duration, nature, objectives, implications, risks and inconveniences of the trial; possible treatment alternatives; and the possible damage compensation system.

Consentement éclairé: avant l’essai, les participants doivent recevoir des informations claires sur leurs droits (y compris le droit de se retirer), les conditions, la durée, la nature, les objectifs, les implications, les risques et les inconvénients de l’essai, d’éventuels traitements alternatifs et d’éventuelles indemnités en cas de dommages.




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Date index: 2024-06-17
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