Übersetzung für "Prescribe medicinal products " (Englisch → Französisch) :

Where medicinal products are authorised within a Member State and have been prescribed in that Member State by a member of a regulated health profession within the meaning of Directive 2005/36/EC for an individual named patient, it should, in principle, be possible for such prescriptions to be medically recognised and for the medicinal products to be dispensed in another Member State in which the medicinal products are authorised.

When a medicinal product has been authorised at Community level [49] the marketing authorisation issued in accordance with Regulation 2309/93 relates to the specific packaging prescribed for the medicinal product in the application for authorisation. The authorisation determines the pack sizes and the immediate packaging to be used for the medicinal product, as well as the information to be included on the immediate or outer packaging [50]. The Court has held that the detailed and specific requirements regarding t ...[+++]he packaging, which are intended to prevent consumers from being misled and, thereby, to protect public health preclude the joining together and re-labelling of packages of that medicinal product [51]. The Court added, however, that the creation of new packaging may be possible if that repackaging is objectively necessary [52] so that the imported product gains effective access to the market of a Member State.

The Court: '1. Declares that, by failing to adopt within the prescribed period the laws, regulations and administrative provisions necessary to comply with Council Directive 92/73/EEC of 22 September 1992 widening the scope of Directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to medicinal products and laying down additional provisions on homeopathic medicinal products, the Kingdom of Belgium has failed to fulf ...[+++]il its obligations under that directive;

- MUTUAL RECOGNITION OF THE VALIDITY OF MEDICAL PRESCRIPTIONS IN THE MEMBER STATES "THE COUNCIL OF THE EUROPEAN UNION, Having regard to the Treaty establishing the European Community, Whereas, in its Resolution of 30 November 1995 on the integration of health protection requirements in Community policies, the Council considers that the Community must pay particular attention to the impact on health of action proposed in a number of areas, including free movement of goods; Whereas action to improve understanding of and address the impact on human health of the free movement of goods, in particular the free movement of medicinal products, should fo ...[+++]rm part of the Community's overall strategy for action in the field of public health; Whereas the internal market comprises an area without internal frontiers in which the free movement of goods, persons, services and capital is ensured; Whereas patients, in moving from one Member State to another, could in practice be prevented from purchasing medicinal products prescribed by an authorized medical practitioner in another Member State; Whereas, pursuant to the Treaty and to Directive 93/16/EEC, all discriminatory treatment based on nationality with regard to establishment and provision of services is prohibited in medical practice; Whereas this Resolution does not affect provisions governing the financing or reimbursement of the cost of medicinal products by national social security schemes; Whereas, moreover, this Resolution does not cover prescriptions for a non-exempt dose of a substance classified as a narcotic drug or psychotropic substance under United Nations international conventions, CALLS on the Commission, in cooperation with the Member States and taking account of work in this area by the relevant international organizations, to look into the present position with regard to the mutual recognition of medical prescriptions in the Member States.

Whereas the provisions of this Directive which concern veterinary medicinal products are, although appropriate, not adequate for veterinary medicinal products used to confer active immunity, to diagnose the state of immunity and to confer passive immunity or for medicinal products based on radioactive isotopes ; whereas it is therefore advisable not to prescribe their application to such products for the present;

- 2 - The Commission takes the view, however, that no restriction should be imposed on (a) imports of medicinal products authorized in a Member State and available there without a prescription, or (b) imports by a private individual for his personal needs of medicinal products lawfully prescribed and purchased in another Member State, whether or not authorized in the Member State of destination.