Vertaling van "european directives regarding medical " (Nederlands → Frans) :

The European directives regarding medical devices are referred to as the New Approach Directives. Products may be commercialised without the intervention of a competent authority.
The European directives regarding medical devices are referred to as the New Approach Directives. Products may be commercialised without the intervention of a competent authority.

De Europese Commissie heeft een voorstel tot “Directive of the European Parliament and of the Council amending, as regards information to the general public on medicinal products subject to medical prescription, Directive 2001l83/EC on the Community code relating to medicinal products for human use” goedgekeurd (bijlage).
La Commission européenne a déposé une proposition de “Directive of the European Parliament and of the Council amending, as regards information to the general public on medicinal products subject to medical prescription, Directive 2001/83/EC on the Community code relating to medicinal products for human use” (cf. annexe).

At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.
At European level, important texts were adopted such as Directive 2007/47/EC amending Directive 93/42/EEC concerning medical devices and Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, and Regulation (EC) no. 1394/2007 on advanced therapy medicinal products.

Medical devices The European medical devices directives are socalled New Approach Directives: the products can be commercialised without the involvement of the competent authorities.
Medical devices The European medical devices directives are socalled New Approach Directives: the products can be commercialised without the involvement of the competent authorities.

The manufacturer also submits a declaration of conformity with the European medical devices directive.
The manufacturer also submits a declaration of conformity with the European medical devices directive.