Vertaling van "market and in clinical development " (Nederlands → Frans) :

To ensure the quality, safety and efficacy of medicines and health products on the market and in clinical development.
To ensure the quality, safety and efficacy of medicines and health products on the market and in clinical development.

Significant investments were made in the first quarter of 2010 in R&D, including post-marketing commitments for A (H1N1) pandemic vaccines as well as the late-stage Menveo and MenB clinical development programs.
Au premier trimestre 2010, des investissements lourds ont été réalisés dans la R&D, comprenant des engagements ultérieurs à la vente pour les vaccins contre la pandémie de grippe A (H1N1) ainsi que des programmes de développement clinique ultime pour les vaccins Menveo et MenB.

Marketing & Sales and R&D both fell as a percentage of net sales despite continued expansion in growth markets and new product development.
En termes de pourcentage du chiffre d’affaires net, les dépenses de Marketing et vente et de R&D ont baissé, malgré la poursuite de l’expansion dans des marchés en pleine croissance et le développement de nouveaux produits.

Novartis ranks as having one of the industry’s most competitive pharmaceuticals development pipelines with 147 projects in clinical development, of which 27 involve new molecular entities in late-stage trials or under regulatory review.
Novartis est considéré comme possédant l’un des pipelines de produits pharmaceutiques les plus concurrentiels de l’industrie avec 147 projets en développement clinique, dont 27 impliquent de nouvelles entités moléculaires qui sont en phase ultime d’essais ou en cours d’examen par les autorités réglementaires.

The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.
The R&D (research and development) department of the FAMHP is responsible for the evaluation and approval of clinical research activities, ranging from the first “use” (concept) to extensive trials with medicines that are developed and carried out by university and other research centres and by the pharmaceutical industry.

FIELDS OF COMPETENCY 19 Activities of the operational departments 20 R&D (research and development) 20 Registration (marketing authorisation) 22 Vigilance 28 Production & Distribution 30 Proper Use of Medicines 38
FIELDS OF COMPETENCY 19 Activities of the operational departments 20 R&D (research and development) 20 Registration (marketing authorisation) 22 Vigilance 28 Production & Distribution 30 Proper Use of Medicines 38

The “PRE pillar” monitors the development of medicines and health products until the point when the initial marketing authorisation (MA) is granted.
The “PRE pillar” monitors the development of medicines and health products until the point when the initial marketing authorisation (MA) is granted.

The FAMHP intends to significantly increase its involvement in the lifecycle of immunological medicines for veterinary use by providing scientific advice, evaluating applications for clinical trials in Belgium, adopting (co-)rapporteurships for CP, MRP and DCP for MA of vaccines for veterinary use and developing pharmacovigilance and inspection activities.
The FAMHP intends to significantly increase its involvement in the lifecycle of immunological medicines for veterinary use by providing scientific advice, evaluating applications for clinical trials in Belgium, adopting (co-)rapporteurships for CP, MRP and DCP for MA of vaccines for veterinary use and developing pharmacovigilance and inspection activities.

The development of a medicine is a continuous process where the finetuning of the chemical–pharmaceutical process and the preclinical and clinical tests both occur in parallel and influence each other.
The development of a medicine is a continuous process where the finetuning of the chemical–pharmaceutical process and the preclinical and clinical tests both occur in parallel and influence each other.

The R&D (research and development) department is required to deal with all relevant applications for clinical trials.
The R&D (research and development) department is required to deal with all relevant applications for clinical trials.