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Assess pharmaceutical manufacturing process
Design pharmaceutical manufacturing systems
Designing pharmaceutical manufacturing systems
Evaluate pharmaceutical manufacturing process
Evaluating pharmaceutical manufacturing process
IFPMA
PMA
Pharmaceutical Manufacturers' Association
Pharmaceutical manufacturing process assessing
Pharmaceutical manufacturing quality systems
Pharmaceutical manufacturing systems design
Pharmaceutical production systems designing
Quality assurance in pharmaceutical manufacture
Quality assurance in pharmaceutical manufacturing
Types of pharmaceutical manufacturing quality systems

Vertaling van "different pharmaceutical manufacturers " (Engels → Frans) :

TERMINOLOGIE
quality assurance in pharmaceutical manufacturing | types of pharmaceutical manufacturing quality systems | pharmaceutical manufacturing quality systems | quality assurance in pharmaceutical manufacture

systèmes de management de la qualité dans la production pharmaceutique


evaluating pharmaceutical manufacturing process | pharmaceutical manufacturing process assessing | assess pharmaceutical manufacturing process | evaluate pharmaceutical manufacturing process

évaluer un procédé de production pharmaceutique


designing pharmaceutical manufacturing systems | pharmaceutical production systems designing | design pharmaceutical manufacturing systems | pharmaceutical manufacturing systems design

concevoir des systèmes de fabrication pharmaceutique


International Federation of Pharmaceutical Manufacturers' Associations | IFPMA [Abbr.]

dération internationale de l'industrie du médicament | FIIM [Abbr.]


International Federation of Pharmaceutical Manufacturers' Associations | IFPMA [Abbr.]

dération internationale de l'industrie du médicament | FIIM [Abbr.]


Pharmaceutical Manufacturers' Association | PMA [Abbr.]

association des industries pharmaceutiques | association des producteurs pharmaceutiques


In EudraLex Volume 4, Guidelines for Good Manufacturing Practice, Medicinal Products for Human and Veterinary Use, Part III: GMP related documents, ICH guideline Q9 on Quality Risk Management (ICH Q9), principles and examples of tools for quality risk management that can be applied to different aspects of pharmaceutical quality, including excipients, can be found.

Dans le volume 4 d’EudraLex, «Guidelines for Good Manufacturing Practice, Medicinal Products for Human and Veterinary Use» (lignes directrices établissant les bonnes pratiques de fabrication, médicaments à usage humain et à usage vétérinaire), partie III, «GMP related documents» (documents liés aux BPF), «ICH guideline Q9 on Quality Risk Management (ICH Q9)» (ligne directrice ICH Q9 relative à la gestion du risque de qualité), on trouve des principes et des exemples d’outils de gestion du risque de qualité qui peuvent être appliqués à différents aspects de la quali ...[+++]


To ensure compliance with good manufacturing practice, thorough inspections of production facilities need to be carried out on a regular basis.The inclusion of excipients within the scope is relevant provided that excipients are addressed separately from active pharmaceutical ingredients and that specific requirements will apply which are different from those applicable to active pharmaceutical ingredients.

Afin de garantir le respect des bonnes pratiques de fabrication, il est nécessaire de procéder régulièrement à des inspections rigoureuses des sites de production. L'extension du champ d'application aux excipients est utile à condition qu'ils soient traités séparément des principes pharmaceutiques actifs et soumis à des exigences spécifiques différentes.


8. Calls for information campaigns to enhance consumers' awareness about products and practices that are harmful during pregnancy, in particular smoking, including second hand smoke, and use of alcohol, but also other consumer goods, such as medicinal products or chemicals, that pose health risks when taken or used during pregnancy; calls on the Commission to encourage manufacturers clearly to state on the packaging of such products that such a risk exists, in order to ensure that pregnant women are properly informed; calls on the European institutions – particularly the European Medicines Agency –, national institutions and consumer organisations to app ...[+++]

8. demande la mise en place de campagnes d'information afin d'accroître la prise de conscience des consommateurs au sujet des pratiques et des produits dangereux durant la grossesse, en particulier le tabagisme – y compris le tabagisme passif – et la consommation d'alcool, mais aussi l'usage d'autres produits tels que les médicaments ou les produits chimiques, présentant un risque pour la santé lorsqu'ils sont consommés ou utilisés pendant la grossesse; invite la Commission à encourager les fabricants à mentionner clairement ce risque sur les emballages des produits, en question de manière à assurer que les femmes enceintes soient convenablement informées; demande aux institutions européennes, et en particulier à l'Agence européenne des m ...[+++]


The manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different departments.

Le fabricant établit et met en oeuvre un système d'assurance de la qualité pharmaceutique efficace, qui implique la participation active de la direction et du personnel des différents services concernés.


The manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different services involved.

Gestion de la qualité Tout fabricant doit instaurer et mettre en application un système efficace d'assurance de la qualité pharmaceutique, impliquant une participation active des responsables et du personnel des divers services.


Quality management The manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different services involved.

Gestion de la qualité Tout fabricant doit instaurer et mettre en application un système efficace d'assurance de la qualité pharmaceutique, impliquant une participation active des responsables et du personnel des divers services.


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