Vertaling van "Implement inspection finished products " (Engels → Nederlands) :

Therefore, this proposal introduce a immediate and definitive testing ban for finished products in the EU and a definitive testing ban for cosmetic ingredients three years after the implementation of this Directive.

1. The competent authorities of collectors and those of the Member States in which processing takes place shall carry out controls comprising physical checks and inspections of commercial documents, with a view to verifying, in the case of collectors, consistency between the purchases of raw materials and the corresponding deliveries, and, in the case of processors, between deliveries respectively of raw materials, finished products, co-produc ...[+++]ts and by-products.

in the case of works contracts, the totality of the technical prescriptions contained in particular in the procurement documents, defining the characteristics required of a material, product or supply, which permits a material, a product or a supply to be described in a manner such that it fulfils the use for which it is intended by the contracting entity; those characteristics include levels of environmental and climate performance, design for all requirements (including accessibility for disabled persons) and conformity assessment, performance, safety or dimensions, including the procedures concerning quality assurance, terminology, s ...[+++]ymbols, testing and test methods, packaging, marking and labelling, user instructions, and production processes and methods at any stage of the life cycle of the works; those characteristics also include rules relating to design and costing, the test, inspection and acceptance conditions for works and methods or techniques of construction and all other technical conditions which the contracting entity is in a position to prescribe, under general or specific regulations, in relation to the finished works and to the materials or parts which they involve;

10. Considers, without prejudice to the application of the procedure provided for in Article 189b, that the objective of the above Community action programme must be to contribute to the fight against drug dependence, in particular by fostering cooperation between Member States, by supporting their action and by promoting the coordination of their prevention policies and programmes, and must include action aimed in particular at: - improving awareness of the problem of drugs and drug dependence and their consequences and of the means and methods of preventing drug dependence and the associated risks, in particular by using the information supplied by the EDMC and the possibilities offered by existing Community programmes and instruments; - contributi ...[+++]ng to the improvement of information, education and training with a view to the prevention of drug dependence and the associated risks, especially for young people and particularly vulnerable groups". BLOOD SAFETY AND SELF-SUFFICIENCY - COUNCIL RESOLUTION "THE COUNCIL OF THE EUROPEAN UNION, RECALLING the Commission communication of 25 May 1993 on blood self- sufficiency in the European Community and its conclusions of 13 December 1993 on that communication; NOTES with interest the Commission communication of 21 December 1994 on blood safety and self-sufficiency in the European Community; REAFFIRMS the need to achieve self-sufficiency in blood and its derivatives in the Member States and in the Community, in particular through cooperation between Member States, in accordance with the principle of voluntary, unpaid blood donations; EMPHASIZES that the efforts to promote the quality and safety of blood collection help to prevent AIDS and other communicable diseases; RECALLS that Directive 89/381/EEC [1] which extends the scope of Directives 65/65/EEC and 75/319/EEC on proprietary medicinal products by laying down special provisions regarding medicines derived from human blood or plasma applies only to these products; ...

VIII. WITH RESPECT TO ACCESS TO THIRD COUNTRY MARKETS 1. underlines the importance of the third-countries market to the pharmaceutical industry of the European Union, which remains the principal world centre for the production and export of medicinal products; 2. considers that, strengthened by the "acquis communautaire" in this sector, the European Union should endeavour to improve the conditions for access to third-country markets for medicinal products invented and developed by the European pharmaceutical industry; 3. points out that the very high degree of regulation in the pharmaceutical sector means that it is also subject to a ...[+++]considerable number of barriers to trade, which often force the pharmaceutical industry to repeat tests on medicinal products and checking operations; 4. notes the efforts made in the context of the International Conference on Harmonization (ICH) with regard to harmonizing statutory requirements for pharmaceuticals and invites the Commission to submit a report to the Council on the results achieved after the first round of conferences and the aims to be set for the continuation of the proceedings; 5. encourages the Commission to continue the negotiations now under way on mutual recognition agreements relating to inspection and control of medicinal products, in particular with regard to equivalence of good manufacturing practice, with the Union's trading partners; 6. recalls the importance of intellectual property rights for the pharmaceutical industry and the crucial part played by effective, complete and respected protection of these rights in ensuring financing for ever more costly innovative research; 7. encourages the fight against fraud and asks the Commission and the Member States to cooperate with the appropriate bodies at international level to combat counterfeiting and ensure the implementation of the agreement on trade-related aspects of intellectual property rights (TRIPs) concluded within the GATT framework; IX. FIN ...

FISHERIES CONTROL - COUNCIL CONCLUSIONS "The Council, having noted the need for greater transparency, coordination and cooperation among Member States in implementing the fisheries control system covering all aspects of the common fisheries policy, as demonstrated in the Commission reports, and the need for efficiently focusing control resources, and taking into account the primary role of the Member States in fisheries control, invites the Member States: - to work together to ensure greater transparency of inspection practices and effec ...[+++]tive and uniform application of Community rules; - to improve mutual understanding of fisheries enforcement in each Member State; - to develop technical cooperation programmes as outlined below; - to take practical steps to improve operational cooperation among the coastal Member State, the flag Member State, and, where appropriate, the Member State of landing, transit and marketing of fisheries products, in the inspection and monitoring of fishing activity and related activities; - to promote better communication and improved understanding among the national control authorities, the scientific community and the fishing industries; - to strengthen coordination and cooperation among Member States in the application of research and new technologies in the domain of control.