Article R5121-51-11
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5121-51-8 and R. 5121-51-9, the Director General of the Agence nationale de sécurité du m…
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Showing 4241–4250 of 6290 articles for “Art. 28 March 2014”
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5121-51-8 and R. 5121-51-9, the Director General of the Agence nationale de sécurité du m…
At the end of the procedures provided for in this sub-section, the marketing authorisation is issued or varied by the Director General of the Agence nationale de sécurité du médicament et des produits…
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
Presenting medical devices that do not comply with the provisions of articles R. 5211-12 and R. 5211-17 at scientific or technical meetings, exhibitions or demonstrations without displaying a sign cle…
…e wording resulting from L. 214-143 to L. 214-150 Order no. 2013-676 of 25 July 2013 L. 214-151 Act 2014-1 of 2 January 2014 L. 214-152 and L. 214-153 Order no. 2013-676 of 25 July 2013 L. 214-154 law…
…f criminal proceedings. II. - I of this Article shall apply to the officers referred to in Articles 28-1,28-1-1 and 28-2. III. - The investigating or trial courts seised of the facts shall have access…
…231-27 and 231-28, the decision to award a classification, a label and a grant is taken after receiving t…
…010 76 of 21 January 2010 L. 613-20-7 Ordinance no. 2015-1024 of 20 August 2015 L. 613-24 Order no. 2014-1332 of 6 November 2014 L. 613-25 Order no. 2019-964 of 18 September 2019 L. 613-26 Order no. 2…
…024/2013 of the Council, and with the Single Resolution Board established by Regulation (EU) No 806/2014 of the European Parliament and of the Council; 4° Third-country authorities performing equivale…
…the meaning of vi of Article 69(a) of Commission Delegated Regulation (EU) No 2015/35 of 10 October 2014 and forms part of the core capital items classified in Tier 1. For the purposes of monitoring t…
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