Traduction de «Nécessaire d'essai du titre des alliages d'or » (Français → Anglais) :

2. Reminds the Council and the Member States that nuclear disarmament and nuclear non-proliferation are substantively interrelated and mutually reinforcing; takes the view that, for the survival and enforcement of the NPT, a road map with a schedule of nuclear disarmament steps and deadlines is needed; urges the nuclear-weapon states to live up to their commitment under Article 6 of the NPT to ‘pursue negotiations in good faith on effective measures relating to cessation of the nuclear arms race at an early date and to nuclear disarmament’; stresses that the nuclear weapon states have not sufficiently lived up to this commitment altho ...[+++]ugh it is vital for the continued relevance of the whole non-proliferation system; calls for strict adherence to the nuclear-testing moratorium pending the entry into force of the Comprehensive Nuclear-Test-Ban Treaty (CTBT);

The emissions tests for roadworthiness purposes set out in Annex IV, tests fuel consumption and CO emissions set out in Annex XII and the requirements for access to vehicle OBD and vehicle repair and maintenance information set out in Annex XIV shall still be required to obtain EC type-approval with regard to emissions and vehicle repair and maintenance information under this paragraph.

Mr. Julian Reed: What I'm getting at is, while I, as a private entrepreneur, might undertake a project that would be subject to this act, certain crown corporations, doing exactly the same thing, would not necessarily be.

2. The holder of a diploma, certificate or other evidence of formal qualifications awarded on completion of a university course - or a course recognized as equivalent by the Member State concerned - in a scientific discipline allowing him to engage in the activities of the person referred to in Article 48 in accordance with the laws of that State may - if he began his course prior to 21 May 1975 - be considered as qualified to carry out in that State the duties of the person referred to in Article 48 provided that he has previously engaged in the following activities for at least two years before 21 May 1985 following notification of this directive ...[+++]in one or more undertakings authorized to manufacture: production supervision and/or qualitative and quantitative analysis of active substances, and the necessary testing and checking under the direct authority of the person referred to in Article 48 to ensure the quality of the medicinal products.

2. The holder of a diploma, certificate or other evidence of formal qualifications awarded on completion of a university course - or a course recognized as equivalent by the Member State concerned - in a scientific discipline allowing him to engage in the activities of the person referred to in Article 52 in accordance with the laws of that State may - if he began his course prior to 9 October 1981 - be considered as qualified to carry out in that State the duties of the person referred to in Article 52, provided that he has previously engaged in the following activities for at least two years before 9 October 1991 in one or ...[+++]more undertakings with a manufacturing authorization; production supervision and/or qualitative and quantitative analysis of active substances, and the necessary testing and checking under the direct authority of a person as referred to in Article 52 to ensure the quality of veterinary medicinal products.

2. The holder of a diploma, certificate or other evidence of formal qualifications awarded on completion of a university course — or a course recognized as equivalent by the Member State concerned — in a scientific discipline allowing him to engage in the activities of the person referred to in Article 52 in accordance with the laws of that State may — if he began his course prior to 9 October 1981 — be considered as qualified to carry out in that State the duties of the person referred to in Article 52, provided that he has previously engaged in the following activities for at least two years before 9 October 1991 in one or ...[+++]more undertakings with a manufacturing authorization; production supervision and/or qualitative and quantitative analysis of active substances, and the necessary testing and checking under the direct authority of a person as referred to in Article 52 to ensure the quality of veterinary medicinal products.