Vertaling van "industrial and developing countries " (Nederlands → Frans) :

Likewise, research carried out up to now has shown that there appears to be a definite connection in all countries, both industrial and developing countries, between alcohol consumption (notably in the Russian Federation and the Baltic states), free access to certain toxic substances (e.g. in China, India and Sri Lanka) and firearms (e.g. in El Salvador and the United States) on the one hand, and the rate of suicide on the other.
De même, la consommation d’alcool (notamment en Fédération de Russie et dans les Etats baltes) ainsi que le libre accès à certaines substances toxiques (en Chine, en Inde et au Sri Lanka, par exemple) et aux armes à feu (à El Salvador et aux Etats-Unis d’Amérique, entre autres) semblent, d’après les études réalisées jusqu’à présent, associés de façon certaine aux taux de suicide dans tous les pays, industrialisés ou en développement.

And there is more: there is also the development of vaccines for developing countries.
And there is more: there is also the development of vaccines for developing countries.

e. Barber shaving and blood-borne disease transmission in developing countries”.
e) Barber shaving and blood-borne disease transmission in developing countries”.

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.

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.

In 2010 vonden op het vlak van contacten met de relevante industrie portfolio/ wetenschappelijke vergaderingen plaats en was er op 18 en 19 november 2010 de CTFG Workshop on Early Phase Development in Oncology.
En 2010, les contacts avec l’industrie concernée ont eu lieu lors des réunions portfolio/scientifiques et lors du CTFG Workshop on Early Phase Development in Oncology (18 et 19 novembre 2010).

Key factor 4 Developing partnerships with the healthcare sector ●● Determining common objectives and priorities with the sector (e.g. professional associations and industry) ●● Determining common objectives and priorities with patients’ associations and members of the public
Key factor 4 Developing partnerships with the healthcare sector ●● Determining common objectives and priorities with the sector (e.g. professional associations and industry) ●● Determining common objectives and priorities with patients’ associations and members of the public

SD/AF/03A (ALLERRISK). Development of an integrated strategy for controlling the allergen issue in the Belgian food and catering industry.
the allergen issue in the Belgian food and catering industry.

Compliance with the European directives on electronic submissions Compliance with the European directives requires a number of objectives to be achieved: ●● Arriving at a functional vision of communication standards with EMEA and the Member States in partnership with the industry and in line with European legislation ●● Standard project management, with important steps that are sponsored/supported by the Member States: first developing an IT infrastructure and then starting on a highly secure network followed by so-called “proofs of concept” in each field ●● Success depends above all on the FAHMP’s
Compliance with the European directives on electronic submissions Compliance with the European directives requires a number of objectives to be achieved: ●● Arriving at a functional vision of communication standards with EMEA and the Member States in partnership with the industry and in line with European legislation ●● Standard project management, with important steps that are sponsored/supported by the Member States: first developing an IT infrastructure and then starting on a highly secure network followed by so-called “proofs of concept” in each field ●● Success depends above all on the FAHMP’s

The “PRE pillar” supports the industry during the development of products, among other means by giving scientific advice and contributing to the compilation of pharmacopoeia monographs.
The “PRE pillar” supports the industry during the development of products, among other means by giving scientific advice and contributing to the compilation of pharmacopoeia monographs.