Vertaling van "development potential " (Nederlands → Frans) :

TERMINOLOGIE

afwijkend(e) | elektro-oculogram [EOG] | afwijkend(e) | elektromyogram [EMG] | afwijkend(e) | elektroretinogram [ERG] | afwijkend(e) | respons op zenuwstimulatie | afwijkend(e) | visually evoked potential [VEP]
Anomalies (de):électromyogramme [EMG] | électro-oculogramme [EOG] | électrorétinogramme [ERG] | potentiels évoqués visuellement | réponse à une stimulation nerveuse

potentiëring | versterking
potentiation/potentialisation | augmentation de l'action d'un médicament par l'absorption d'un second

potentie | kracht
1) puissance sexuelle - 2) efficacité | 1) puissance sexuelle - 2) d'un médicament

IN-CONTEXT TRANSLATIONS

These were: industrial fabric in Belgium, research and expertise in Belgium, expertise within the FAMHP, development potential, differentiating potential and speed with which expertise can be developed.
These were: industrial fabric in Belgium, research and expertise in Belgium, expertise within the FAMHP, development potential, differentiating potential and speed with which expertise can be developed.

This release contains forward-looking information about an agreement by Pfizer to acquire FoldRx, and about FoldRx’s product candidate tafamidis, its other clinical and preclinical development programs and its technology platform, including their potential benefits, that involves substantial risks and uncertainties. Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009 and in its reports on Form 10-Q and Form 8-K.
Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments.

Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments.
This release contains forward-looking information that involves substantial risks and uncertainties regarding Prevenar 13, including its potential benefits; and the success of the AMC project for vaccines. Such risks and uncertainties include, among other things, the uncertainties inherent in research and development; whether and when regulatory authorities in countries where regulatory applications for Prevenar 13 may be pending or may be submitted will approve such applications and their decisions regarding labeling and other matters that could affect its availability or commercial potential; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009, and in its reports on Form 10-Q and Form 8-K.

Pharmaceuticals – Protez On June 4, Novartis agreed to acquire Protez Pharmaceuticals, a privately held US biopharmaceuticals company, gaining access to PTZ601, a broad-spectrum antibiotic in Phase II development against potentially fatal drug-resistant bacterial infections.
Pharmaceuticals – Protez Le 4 juin, Novartis a convenu d’acquérir Protez Pharmaceuticals, une société américaine de biotechnologie en mains privées. Cet accord a permis à Novartis d’accéder à PTZ-601, un antibiotique à large spectre en phase II de développement pour traiter des infections bactériennes potentiellement fatales qui résistent aux médicaments.

In the same train of thought, a very recent report of the Committee on Toxicity of Chemicals in Food, an independent scientific advisory body in the United Kingdom, shows the state of affairs concerning the potential toxicity of caffeine in pregnant women and affirms, with great circumspection, that caffeine is already likely to affect the development of the foetus from a daily consumption of 200 mg (COT, 2008).
Dans le même ordre d’idées, un rapport très récent du Comité de Toxicologie du Royaume-Uni, organisme indépendant de conseil scientifique, fait un nouveau point sur la possible toxicité de la caféine chez la femme enceinte et déclare, avec beaucoup de précautions, qu’il est vraisemblable que la caféine affecte le développement du fœtus déjà pour des apports journaliers de l’ordre de 200 mg (COT, 2008).