Traduction de «approved laboratory » (Anglais → Français) :

(b) individual fluff samples or such other samples as may be required by an inspector from each hatcher in the hatchery are submitted by the owner or operator of the hatchery to an approved laboratory for testing every sixth week as follows:

79.2 Every owner or person in charge of a chicken, turkey or game bird that on serological testing shows a reaction that may indicate exposure to or the presence of Salmonella pullorum or Salmonella gallinarum shall immediately submit the chicken, turkey or game bird to an approved laboratory for culturing or further testing.

1. Where it considers it necessary, a Member State may require the marketing authorization holder for immunological products to submit samples from the batches of the bulk and/or medical product for examination by a State laboratory or an approved laboratory before entry into circulation.

Member States shall send the Commission a list of approved laboratories, specifying the criteria used for approval and the methods of monitoring applied, by 30 September 2002, and whenever any change is made.

The residue monitoring plan of the US, particularly regarding approved laboratories to which certain analytical work could be contracted out, was updated by the US and the arrangements made concerning approved laboratories to which certain analytical work was contracted out was communicated to the European Commission.

- 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.