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Administer the logistics of medicinal products
Ethical drug
Fabricate medicines
Formulate medicines
Generic
Generic drug
Generic medicament
Generic medicinal product
Generic medicine
Generic pharmaceutical
Generic pharmaceutical product
Handle the logistics of medicinal products
Manage the logistics of medicinal products
Manufacture medicines
Manufacture pharmaceutical products
Medicinal product for veterinary use
Medicinal product not subject to medical prescription
Medicinal product subject to medical prescription
Non-prescription drug
Non-prescription medicinal product
Non-proprietary medicinal product
OTC drug
OTC medicine
Over-the-counter drug
Over-the-counter medicine
P&R policy
POM
Pharmaceutical pricing and reimbursement
Pharmaceutical pricing policy
Pharmaceutical reimbursement and pricing policy
Prepare medication according to prescriptions
Prepare medication from prescription
Prepare medicinal products from prescription
Prescription drug
Prescription medicine
Prescription only medicine
Prescription-only medicinal product
Pricing and reimbursement of medicinal products
Pricing of medicines
Rx drug
VMP
VMPO
Veterinary Medicinal Products Ordinance
Veterinary medicinal product
Veterinary pharmaceutical product
Veterinary product

Vertaling van "medicinal products often " (Engels → Frans) :

TERMINOLOGIE
ensure storage, preservation and distribution of medicinal products | handle the logistics of medicinal products | administer the logistics of medicinal products | manage the logistics of medicinal products

gérer la logistique des produits médicaux


veterinary medicinal product [ medicinal product for veterinary use | veterinary pharmaceutical product | veterinary product | VMP ]

produit vétérinaire [ produit à usage vétérinaire ]


generic | generic drug | generic medicament | generic medicinal product | generic medicine | generic pharmaceutical | generic pharmaceutical product | non-proprietary medicinal product

générique | médicament générique | produit pharmaceutique générique


ethical drug | medicinal product subject to medical prescription | prescription drug | prescription medicine | prescription only medicine | prescription-only medicinal product | Rx drug | POM [Abbr.]

médicament de prescription | médicament délivré uniquement sur prescription médicale | médicament soumis à prescription | médicament soumis à prescription médicale


medicinal product not subject to medical prescription | non-prescription drug | non-prescription medicinal product | OTC drug | OTC medicine | over-the-counter drug | over-the-counter medicine

médicament en vente libre | médicament grand public


over-the-counter drug [ non-prescription drug | non-prescription medicinal product | OTC drug | OTC medicine | over-the-counter medicine ]

médicament en vente libre [ médicament non soumis à prescription | médicament sans ordonnance | MSO ]


pricing of medicines [ P&R policy | pharmaceutical pricing and reimbursement | pharmaceutical pricing policy | pharmaceutical reimbursement and pricing policy | pricing and reimbursement of medicinal products ]

fixation des prix des médicaments [ fixation des prix et remboursement des produits pharmaceutiques | politique de fixation des prix des produits pharmaceutiques | politique de fixation des prix et de remboursement des médicaments ]


fabricate medicines | formulate medicines | manufacture medicines | manufacture pharmaceutical products

fabriquer des médicaments


Ordinance of 18 August 2004 on Veterinary Medicinal Products | Veterinary Medicinal Products Ordinance [ VMPO ]

Ordonnance du 18 août 2004 sur les médicaments vétérinaires [ OMédV ]


prepare medicinal products from prescription | prepare pharmaceutical form of medication from prescription | prepare medication according to prescriptions | prepare medication from prescription

préparer des médicaments selon une prescription
IN-CONTEXT TRANSLATIONS
The evaluation of advanced therapy medicinal products often requires very specific expertise, which goes beyond the traditional pharmaceutical field and covers areas bordering on other sectors such as biotechnology and medical devices.

L’évaluation des médicaments de thérapie innovante demande souvent une expertise très spécifique, qui va au-delà du domaine pharmaceutique traditionnel et comprend des aspects à la frontière d’autres disciplines, telles que la biotechnologie et les dispositifs médicaux.


Studies necessary to demonstrate the quality and non-clinical safety of advanced therapy medicinal products are often carried out by small and medium-sized enterprises.

Les études nécessaires pour démontrer la qualité et la sécurité non clinique des médicaments de thérapie innovante sont souvent réalisées par des petites et moyennes entreprises.


This is due to the long development cycles of medicinal products, often lasting more than a decade and the near-systematic deferral of paediatric studies.

Cette situation s’explique par les longs cycles de conception des médicaments, qui durent couramment plus d’une décennie, et par le report pratiquement systématique des études pédiatriques.


Clinical trials for the development of orphan medicinal products as defined in Regulation (EC) No 141/2000 of the European Parliament and of the Council and of medicinal products addressed to subjects affected by severe, debilitating and often life-threatening diseases affecting no more than one person in 50 000 in the Union (ultra-rare diseases) should be fostered.

Il convient d'encourager les essais cliniques pour la mise au point de médicaments orphelins au sens du règlement (CE) no 141/2000 du Parlement européen et du Conseil et de médicaments destinés aux patients atteints de maladies lourdes, invalidantes et, souvent, mettant la vie en danger qui ne touchent pas plus d'une personne sur 50 000 dans l'Union (maladies ultra-rares).


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Clinical trials for the development of orphan medicinal products as defined in Regulation (EC) No 141/2000 of the European Parliament and of the Council (4) and of medicinal products addressed to subjects affected by severe, debilitating and often life-threatening diseases affecting no more than one person in 50 000 in the Union (ultra-rare diseases) should be fostered.

Il convient d'encourager les essais cliniques pour la mise au point de médicaments orphelins au sens du règlement (CE) no 141/2000 du Parlement européen et du Conseil (4) et de médicaments destinés aux patients atteints de maladies lourdes, invalidantes et, souvent, mettant la vie en danger qui ne touchent pas plus d'une personne sur 50 000 dans l'Union (maladies ultra-rares).


Those low-intervention clinical trials are often of crucial importance for assessing standard treatments and diagnoses, thereby optimising the use of medicinal products and thus contributing to a high level of public health.

Ces essais cliniques à faible niveau d'intervention sont souvent d'une importance fondamentale pour l'évaluation de traitements et de diagnostics standards, en ce sens qu'ils optimisent l'utilisation des médicaments et contribuent ainsi à garantir un niveau élevé de santé publique.


Additionally, in contrast to chemical-based medicinal products, research in advanced therapies is -for the most part- conducted by academia, non-for-profit organisations, and SMEs, which only have limited financial resources and often lack exposure to the regulatory system that governs medicines.

En outre, à la différence des médicaments chimiques, la recherche en matière de thérapies innovantes est majoritairement conduite par des universités, des organisations sans but lucratif et des PME qui n’ont que peu de ressources financières et connaissent souvent mal le système réglementaire applicable aux médicaments.


Since the adoption of this Directive, market conditions have fundamentally changed, for instance with the emergence of generic medicines providing cheaper versions of existing products or the development of increasingly innovative (yet often expensive) research-based medicinal products.

Depuis l’adoption de cette directive, les conditions du marché ont profondément changé, par exemple avec l’émergence de médicaments génériques constituant des versions moins coûteuses de médicaments existants ou avec le développement de médicaments de plus en plus novateurs (mais souvent plus coûteux), fruits d’un travail de recherche.


The evaluation of advanced therapy medicinal products often requires very specific expertise, which goes beyond the traditional pharmaceutical field and covers areas bordering on other sectors such as biotechnology and medical devices.

L’évaluation des médicaments de thérapie innovante demande souvent une expertise très spécifique, qui va au-delà du domaine pharmaceutique traditionnel et comprend des aspects à la frontière d’autres disciplines, telles que la biotechnologie et les dispositifs médicaux.


This is due to the long development cycles of medicinal products, often lasting more than a decade and the near-systematic deferral of paediatric studies.

Cette situation s’explique par les longs cycles de conception des médicaments, qui durent couramment plus d’une décennie, et par le report pratiquement systématique des études pédiatriques.


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