Article L1111-3-2
…e procedure includes the supply of a custom-made device referred to in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 concerning medical devices, a…
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Showing 1451–1460 of 3003 articles for “Art. 31 janv. 2017”
…e procedure includes the supply of a custom-made device referred to in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 concerning medical devices, a…
…ance and Reinsurance (Solvency II), in the version in force on the date of publication of Decree No 2017-1171 of 18 July 2017 laying down the rules applicable to supplementary occupational pension fun…
…poses and its annexes; 4° The provisions of Articles 1 to 7 of Commission Delegated Regulation (EU) 2017/1798 of 2 June 2017 supplementing Regulation (EU) No 609/2013 of 12 June 2013 as regards the sp…
…qual to one, increased by the ratio between twice the population of sensitive urban areas and, from 2017, priority neighbourhoods of the city policy and the total population of the municipality, and t…
…ssories intended to perform self-diagnostics, as defined in point 5 of Article 2 of Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017, for the detection of transmi…
…bear the secure electronic signature of the registrar who drew them up, as defined by the décret n° 2017-1416 du 28 septembre 2017 relatif à la signature électronique; 4°They must be stored under cond…
…Law no. 2021-1308 of 8 October 2021 L. 330-3 Order no. 2009-866 of 15 July 2009 L. 330-4 Order no. 2017-1252 of 9 August 2017 II.For the application of I: 1° References to EU Regulations No 648/2012…
The liquidation of the company under the conditions provided for in articles L. 237-15 to L. 237-31 is ordered by the President of the Commercial Court, ruling in summary proceedings, at the request o…
…plication of II of article L. 23-111-1, branches for which an agreement was concluded no later than 31 March of the year in which the regional cross-industry joint committee was set up or renewed are…
…ic health establishments must prove that they were manufacturing medicinal products industrially on 31 December 1991 and specify the nature and quantities of medicinal products manufactured annually.
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