Traduction de «procédure de laboratoire » (Français → Anglais) :

Following the completion of a selection procedure, the successful laboratory, Agence Nationale de Sécurité Sanitaire de l’alimentation, de l’environnement et du travail (ANSES), with its research laboratory for bee diseases, Sophia-Antipolis Laboratory, France, should be designated as the EU reference laboratory in the field of bee health, for a period of five years from 1 April 2011.

(f) laboratory procedures and methods of analysis; and

(g)where applicable, a list of laboratories engaged in carrying out relevant analytical procedures and, where the laboratory is not accredited as referred to in Article 34(1) a description of the procedure used for demonstrating the compliance with equivalent requirements in accordance with Article 34(2) and (3).

Perhaps the hon. member is in a position to answer the question (1240) Mr. James Lunney: Mr. Speaker, I know that as an authority in his own right in laboratory medicine and procedures, his question is a genuine one.

Scientific issues arising in the area of infectious diseases vary widely, ranging from questions of clinical medicine and epidemiology through to standardisation of laboratory procedures.

- 2 - The approach adopted by the directive includes the following main points: - any terminal certified as conforming with the technical requirements will be authorized for marketing; - the "right of connection" to public telecommunications networks in the Community will be guaranteed for certified equipment, without the need for repeated testing and approval procedures; - the tests will be carried out and approval issued by approved laboratories and certification bodies set out in a Community list. To be on this list laboratories and bodies must meet strict criteria of competence, impartiality and independence which are harmonized at ...[+++] Community level; - the certificates of conformity issued under the procedure laid down by the Directive will be fully recognized in all Member State; - to assess conformity manufacturers will have the choice of two procedures, the EEC type-approval examination and the EEC declaration of conformity; - manufacturers will have the right to choose the laboratory or body that carries out the tests for conformity with the common technical specifications on their equipment. Accreditation of the laboratory of the manufacturer is possible as long as it satisfies the selection criteria; - the directive demands that the Member States should take all suitable measures to ensure that only terminals which meet the requirements set out in the directive are marketed. The Member States may take measures to disconnect any equipment which is not approved; - certified equipment will all bear an identical mark, namely, the "EC" mark, and other distinctive symbols making them readily identifiable.