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Carry out toxicological studies
Clinical toxicology of commercial products
Create safe working protocols
Create working protocols for safety
Develop working protocols according to guidelines
Inhalation toxicology
Perform toxicological studies
Perform toxicological study
Perform toxicological tests
Pharmaco-toxicological protocol
Protocols and Toxicology
Respiratory toxicology
STIC
Set safety working protocols
Swiss Poison Centre
Swiss Toxicological Information Center
Swiss Toxicological Information Centre
Toxicologist
Toxicology Assessment and Ecological Protocols Division
Toxicology research scientist
Toxicology scientist
Toxicology studies research scientist

Translation of "Protocols and Toxicology " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Protocols and Toxicology
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
Protocoles et toxicologie
Various Proper Names
Appellations diverses
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
perform toxicological study | perform toxicological tests | carry out toxicological studies | perform toxicological studies
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
réaliser des études toxicologiques
skill
Aptitude
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
pharmaco-toxicological protocol
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
protocole toxico-pharmacologique
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
pharmaco-toxicological protocols/standards
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
normes toxicopharmacologiques | toxico-vigilance
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Toxicology Assessment and Ecological Protocols Division
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
Division des évaluations toxicologiques et des protocoles écologiques
National Bodies and Committees (Canadian) | Ecology (General)
Organismes et comités nationaux canadiens | Écologie (Généralités)
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
toxicology research scientist | toxicology scientist | toxicologist | toxicology studies research scientist
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
toxicologiste | toxicologue | toxicologue de l’industrie
Professionals
Professions intellectuelles et scientifiques
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
inhalation toxicology | respiratory toxicology
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
toxicologie respiratoire
IATE -
IATE -
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Clinical toxicology of commercial products: acute poisoning [ Clinical toxicology of commercial products ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
Clinical toxicology of commercial products: acute poisining [ Clinical toxicology of commercial products ]
Titles of Documents and Works
Titres de documents et d'œuvres
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http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Swiss Toxicological Information Centre (1) | Swiss Toxicological Information Center (2) | Swiss Poison Centre (3) [ STIC ]
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
Centre Suisse d'Information Toxicologique | Centre anti-poison [ CSIT ]
Medicine & biology
Organismes (Sciences médicales et biologiques) | Pharmacologie - toxicologie (Sciences médicales et biologiques)
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
https://www.termdat.bk.admin.c (...) [HTML] [2018-01-01]
develop working protocols according to guidelines | set safety working protocols | create safe working protocols | create working protocols for safety
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
créer des protocoles de travail en toute sécurité
skill
Aptitude
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
IN-CONTEXT TRANSLATIONS
Gray LE Jr, Furr J and Ostby JS (2005). Hershberger assay to investigate the effects of endocrine disrupting compounds with androgenic and antiandrogenic activity in castrate-immature male rats. In: Current Protocols in Toxicology 16.9.1-16.9.15. J Wiley and Sons Inc.
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2013-12-31]
Gray, L.E. Jr, Furr, J., et Ostby, J.S (2005), Hershberger assay to investigate the effects of endocrine disrupting compounds with androgenic and antiandrogenic activity in castrate-immature male rats, in Current Protocols in Toxicology, 16.9.1-16.9.15, J. Wiley and Sons Inc.
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2013-12-31]
http://eur-lex.europa.eu/legal (...) [HTML] [2013-12-31]
Council Directive 81/851/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to veterinary medicinal products , Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products , Council Directive 90/677/EEC of 13 December 1990 extending the scope of Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products and laying down additional provisions for immunological vet ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-11-05]
La directive 81/851/CEE du Conseil du 28 septembre 1981 concernant le rapprochement des législations des États membres relatives aux médicaments vétérinaires , la directive 81/852/CEE du Conseil du 28 septembre 1981 relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicaments vétérinaires , la directive 90/677/CEE du Conseil du 13 décembre 1990 élargissant le champ d'application de la directive 81/851/CEE concernant le rapprochement des législations des États membres relatives aux médicaments vétérinaires et prévoyant ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-11-05]
https://eur-lex.europa.eu/lega (...) [HTML] [2001-11-05]
(1) Council Directive 81/851/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to veterinary medicinal products(3), Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products(4), Council Directive 90/677/EEC of 13 December 1990 extending the scope of Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products and laying down additional provisions for immunolog ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-11-05]
(1) La directive 81/851/CEE du Conseil du 28 septembre 1981 concernant le rapprochement des législations des États membres relatives aux médicaments vétérinaires(3), la directive 81/852/CEE du Conseil du 28 septembre 1981 relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicaments vétérinaires(4), la directive 90/677/CEE du Conseil du 13 décembre 1990 élargissant le champ d'application de la directive 81/851/CEE concernant le rapprochement des législations des États membres relatives aux médicaments vétérinaires et pr ...[+++]
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https://eur-lex.europa.eu/lega (...) [HTML] [2001-11-05]
(a) the format and contents of the request referred to in paragraph 2 as well as the documentation to be submitted to support that request, on the quality and manufacture of the investigational medicinal product, any toxicological and pharmacological tests, the protocol and clinical information on the investigational medicinal product including the investigator's brochure.
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-04-03]
a) la présentation et le contenu de la demande visée au paragraphe 2, ainsi que les documents à fournir à l'appui de cette demande, portant sur la qualité et la fabrication du médicament expérimental, les essais toxicologiques et pharmacologiques, le protocole et les informations cliniques relatives au médicament expérimental, notamment la brochure pour l'investigateur.
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-04-03]
https://eur-lex.europa.eu/lega (...) [HTML] [2001-04-03]
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(1) Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by law, regulation or administrative action relating to medicinal products(4) requires that applications for authorisation to place a medicinal product on the market should be accompanied by a dossier containing particulars and documents relating to the results of tests and clinical trials carried out on the product. Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2001-04-03]
(1) La directive 65/65/CEE du Conseil du 26 janvier 1965 concernant le rapprochement des dispositions législatives, réglementaires et administratives, relatives aux médicaments(4) dispose que les demandes d'autorisation de mise sur le marché d'un médicament sont accompagnées d'un dossier contenant les renseignements et les documents relatifs aux résultats des tests et des essais cliniques réalisés sur ce produit; la directive 75/318/CEE du Conseil du 20 mai 1975 relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicam ...[+++]
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https://eur-lex.europa.eu/lega (...) [HTML] [2001-04-03]
(7) Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of medicinal products (OJ L 147, 9.6.1975, p. 1).
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2000-11-15]
(7) Directive 75/318/CEE du Conseil du 20 mai 1975 relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicaments (JO L 147 du 9.6.1975, p. 1).
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https://eur-lex.europa.eu/lega (...) [HTML] [2000-11-15]
(7) Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of medicinal products (OJ L 147, 9.6.1975, p. 1).
http://eur-lex.europa.eu/legal (...) (...) [HTML] [1999-12-31]
(7) Directive 75/318/CEE du Conseil du 20 mai 1975 relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicaments (JO L 147 du 9.6.1975, p. 1).
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http://eur-lex.europa.eu/legal (...) [HTML] [1999-12-31]
Whereas the principles and guidelines envisaged by this Directive are in conformity with the opinion of the Committee for Adaptation of Technical Progress of the Directives on the Removal of Technical Barriers to Trade in the Veterinary Medicinal Products Sector created by Article 2b of Directive 81/852/EEC of 28 September 1981 concerning the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products (4), as last amended by Directive 87/20/EEC (5),
http://eur-lex.europa.eu/legal (...) (...) [HTML] [1990-12-31]
considérant que les principes et lignes directrices prévus par la présente directive sont conformes à l'avis du comité pour l'adaptation au progrès technique des directives visant à l'élimination des entraves techniques aux échanges dans le secteur des médicaments vétérinaires, institué par l'article 2 ter de la directive 81/852/CEE du Conseil, du 28 septembre 1981, relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de m ...[+++]
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Whereas the principles and guidelines envisaged by this Directive are in accordance with the opinion of the Committee for the Adaptation to Technical Progress of the Directives on the Removal of Technical Barriers to Trade in the Proprietary Medicinal Products Sector set up by Article 2b of Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products (3), as last amended by Directive 89/341/EEC (4),
http://eur-lex.europa.eu/legal (...) (...) [HTML] [1990-12-31]
considérant que les principes et lignes directrices prévus par la présente directive sont conformes à l'avis du comité pour l'adaptation au progrès technique des directives visant à l'élimination des entraves techniques aux échanges dans le secteur des médicaments, institué par l'article 2 ter de la directive 75/318/CEE du Conseil, du 20 mai 1975, relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et cliniques en matière d'essais de médicaments (3), mod ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [1990-12-31]
http://eur-lex.europa.eu/legal (...) [HTML] [1990-12-31]
Whereas Community rules regarding veterinary medicinal products, and in particular Council Directive 81/851/EEC of 28 September 1981 on the approximation of the laws of Member States relating to veterinary medicinal products (4), and Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products (5), as amended by Directive 87/20/EEC (6), should be taken into account;
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considérant que, ce faisant, il convient de tenir compte des réglementations communautaires concernant les médicaments vétérinaires, et en particulier de la directive 81/851/CEE du Conseil, du 28 septembre 1981, concernant le rapprochement des dispositions législatives des États membres relatives aux médicaments vétérinaires (4), et la directive 81/852/CEE du Conseil, du 28 septembre 1981, relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico-pharmacologiques et vétérinaires ou cliniques en matière d'essais de médicaments vétérinaires (5), modifiée par la directive 87/20/CEE ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [1989-12-31]
http://eur-lex.europa.eu/legal (...) [HTML] [1989-12-31]


Others have searched : clinical toxicology of commercial products    protocols and toxicology    swiss poison centre    swiss toxicological information center    swiss toxicological information centre    carry out toxicological studies    create safe working protocols    create working protocols for safety    inhalation toxicology    perform toxicological studies    perform toxicological study    perform toxicological tests    respiratory toxicology    set safety working protocols    toxicologist    toxicology research scientist    toxicology scientist    toxicology studies research scientist    Protocols and Toxicology    


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'Protocols and Toxicology'

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