Article R784-6
…articlesIn the wording resulting from the decreeR. 612-22, R. 612-24 and R. 612-25No. 2010-217 of 3 March 2010R. 612-26No. 2011-769 of 28 June 2011R. 612-27n° 2014-1315 of 3 November 2014R. 612-28n° 2…
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Showing 931–940 of 6073 articles for “Art. 28 March 2012”
…articlesIn the wording resulting from the decreeR. 612-22, R. 612-24 and R. 612-25No. 2010-217 of 3 March 2010R. 612-26No. 2011-769 of 28 June 2011R. 612-27n° 2014-1315 of 3 November 2014R. 612-28n° 2…
Without prejudice to Titles III, IV or V of Regulation (EU) No 648/2012 of the European Parliament and of the Council of 4 July 2012 on OTC derivatives, central counterparties and trade repositories,…
…of a marketing authorisation for a medicinal product granted under 1°, 2° or 3° of article R. 5121-28, prior to the marketing of the medicinal product or speciality concerned, of the fact that for so…
…lting from this chapter, the Agency's financial system is set out in Titles I and III of Decree No. 2012-1246 of 7 November 2012 on public budget management and accounting. The Agency's budget shall g…
…not admitted to trading on a financial instruments market within the meaning of I of Article L. 214-28 or in entities referred to in 2° of II of Article L. 214-28 or in venture capital funds referred…
…r, on the date referred to in III of Article L. 211-17. Without prejudice to Regulation (EU) No 236/2012 of the European Parliament and of the Council of 14 March 2012 on short selling and certain asp…
…ntial requirements for credit institutions and investment firms and amending Regulation (EU) No 648/2012, shall take into account at least one of the following criteria: -financial instruments and rel…
…of, on behalf of and in the name of the State, the guarantees provided for inArticle 84 of Act No. 2012-1510 of 29 December 2012 amending the Finance Act for 2012.
…e presentation and content of which are laid down in accordance with Article 14 of Directive 2004 / 28 / EC of 31 March 2004 by order of the Ministers for Agriculture and Health on a proposal from the…
…y operator of such a medicinal product is required, within one year of the promulgation of Act 2011-2012 of 29 December 2011 on reinforcing the safety of medicinal products and health products, to mak…
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