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Apply good clinical practice
Apply good clinical practices
Apply good clinical trial practice
Assistant pharmaceutical goods distribution manager
Code of good agricultural practice
Code of good farming practice
GAP
GDP
Good agricultural practice
Good agricultural practices
Good distribution practice
Graduate household goods distribution manager
Graduate pharmaceutical goods distribution manager
Household goods distribution manager
Household goods distribution planner
Meet good clinical practice standards
Pharmaceutical goods distribution manager
Senior household goods distribution manager
Senior pharmaceutical goods distribution manager
Usual good farming practice

Vertaling van "good distribution practice " (Engels → Frans) :

TERMINOLOGIE
good distribution practice | GDP [Abbr.]

bonne pratique de distribution


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

appliquer la bonne pratique clinique


good agricultural practice | good agricultural practices | usual good farming practice | GAP [Abbr.]

bonne pratique agricole | bonnes pratiques agricoles | BPA [Abbr.]


assistant pharmaceutical goods distribution manager | senior pharmaceutical goods distribution manager | graduate pharmaceutical goods distribution manager | pharmaceutical goods distribution manager

responsable de la logistique distribution de produits pharmaceutiques


graduate household goods distribution manager | household goods distribution planner | household goods distribution manager | senior household goods distribution manager

responsable de la logistique distribution d'articles ménagers


code of good agricultural practice | code of good farming practice

code de bonne conduite agricole | code de bonne pratique agricole | code de bonnes pratiques agricoles


These Guidelines replace the Guidelines on Good Distribution Practice of medicinal products for human use, published on 1 March 1994 and the Guidelines of 7 March 2013 on Good Distribution Practice of medicinal products for human use

Les présentes lignes directrices remplacent les lignes directrices concernant les bonnes pratiques de distribution en gros des médicaments à usage humain, publiées le 1er mars 1994 , et les lignes directrices du 7 mars 2013 concernant les bonnes pratiques de distribution en gros des médicaments à usage humain


These include requirements relating to the existence of suitable premises, installations and equipment, qualified staff to ensure proper conservation and distribution of medicinal products, the documentation of transactions, the supply of medicinal products and compliance with good distribution practice.

Il s'agit, notamment, des exigences relatives à l’existence de locaux, d’installations et d’équipements adaptés, d’un personnel qualifié de façon à assurer une bonne conservation et une bonne distribution des médicaments, d’une documentation de transactions, de la fourniture de médicaments et de l'observation des bonnes pratiques de distribution.


5. Within 90 days of an inspection as referred to in paragraph 1, a certificate of good manufacturing practice or good distribution practices shall, when applicable, be issued to the inspected entity if the outcome of the inspection shows that it complies with the principles and guidelines of good manufacturing practice or good distribution practices as provided for by Union legislation.

5. Dans les quatre-vingt-dix jours suivant une inspection visée au paragraphe 1, un certificat de bonnes pratiques de fabrication ou de distribution est délivré, le cas échéant, à l’entité inspectée, si l’inspection aboutit à la conclusion qu’elle respecte les principes et lignes directrices de bonnes pratiques de fabrication ou de distribution prévus par la législation de l’Union.


to comply with the principles and guidelines of good manufacturing practice for medicinal products and to use only active substances, which have been manufactured in accordance with good manufacturing practice for active substances and distributed in accordance with good distribution practices for active substances.

de respecter les principes et lignes directrices de bonnes pratiques de fabrication des médicaments et d’utiliser seulement des substances actives fabriquées conformément aux bonnes pratiques de fabrication des substances actives et distribuées conformément aux bonnes pratiques de distribution des substances actives.


Furthermore, the manufacturers of medicinal products must verify that the manufacturer and the distributor of the respective active substances comply with good manufacturing practice and good distribution practices.

En outre, les fabricants de médicaments doivent vérifier que le fabricant et le distributeur des substances actives concernées respectent les bonnes pratiques de fabrication et de distribution.


5. Within 90 days of an inspection as referred to in paragraph 1, a certificate of good manufacturing practice or good distribution practices shall, when applicable, be issued to the inspected entity if the outcome of the inspection shows that it complies with the principles and guidelines of good manufacturing practice or good distribution practices as provided for by Union legislation.

5. Dans les quatre-vingt-dix jours suivant une inspection visée au paragraphe 1, un certificat de bonnes pratiques de fabrication ou de distribution est délivré, le cas échéant, à l’entité inspectée, si l’inspection aboutit à la conclusion qu’elle respecte les principes et lignes directrices de bonnes pratiques de fabrication ou de distribution prévus par la législation de l’Union.


(f)to comply with the principles and guidelines of good manufacturing practice for medicinal products and to use only active substances, which have been manufactured in accordance with good manufacturing practice for active substances and distributed in accordance with good distribution practices for active substances.

f)de respecter les principes et lignes directrices de bonnes pratiques de fabrication des médicaments et d’utiliser seulement des substances actives fabriquées conformément aux bonnes pratiques de fabrication des substances actives et distribuées conformément aux bonnes pratiques de distribution des substances actives.


The Commission's Joint Research Centre (the "ECVAM" facility, or "European Centre for Validation of Alternative Methods") played a major role in the project through provision of scientific and technical advice on the design of the validation study, application of good laboratory practice procedures and distribution and coding of test material.

Le Centre commun de recherche de la Commission (par l'intermédiaire du CEVMA ou "Centre européen pour la validation des méthodes alternatives") a joué un rôle capital dans le projet, qu'il s'agisse de donner des conseils scientifiques et techniques sur la conception de l'étude de validation, d'appliquer des procédures de bonnes pratiques de laboratoire et de diffuser et coder le matériel d'essai.


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