Article R1335-8-1
…om healthcare activities with infectious risks meeting the requirements of a of 2° of Article R. 1335-1; 2° Medicinal product: any medicinal product within the meaning of Article L. 5111-1, whether or…
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Showing 9111–9120 of 18177 articles for “Art. 5 oct. 2017”
…om healthcare activities with infectious risks meeting the requirements of a of 2° of Article R. 1335-1; 2° Medicinal product: any medicinal product within the meaning of Article L. 5111-1, whether or…
…be signed using a qualified electronic signature process that meets the requirements of Decree No. 2017-1416 of 28 September 2017 on electronic signatures.Withdrawal of the qualification of one or mo…
…with one or more companies falling within the scope of paragraph 1 of Article 160b of Directive EU 2017/1132 of the European Parliament and of the Council of 14 June 2017 on certain aspects of compan…
…ensure the identification and traceability of the devices mentioned in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 concerning medical devices, a…
…ioned in I of Article 1498: 1° Partial exemptions from direct local taxes are granted for the years 2017 to 2025 when the difference between the assessment established for the year 2017 in application…
…es to Regulations (EU) of the European Parliament and of the Council No 648/2012 of 4 July 2012, No 575/2013 of 26 June 2013, No 596/2014 of 16 April 2014, No 600/2014 of 15 May 2014, No 909/2014 of 2…
…hand column of the same table: Articles applicable In the wording resulting from L. 322-1 Order no. 2017-1107 of 22 June 2017 L. 322-2 to L. 322-10 Order no. 2015-1024 of 20 August 2015 II.-For the ap…
…es to Regulations (EU) of the European Parliament and of the Council No 648/2012 of 4 July 2012, No 575/2013 of 26 June 2013, No 596/2014 of 16 April 2014, No 600/2014 of 15 May 2014, No 909/2014 of 2…
…ticles L. 242-10 to L. 242-13, following a request for mutual assistance provided for in Article L. 511-10 relating to a large-scale or EU-wide infringement, pursuant to Article 21 of Regulation (EU)…
…turer, authorised representative or importer of devices referred to in Article 1 of Regulation (EU) 2017/746, whose registered office is located on French territory, to register the device or update t…
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