Article L5142-1-1
…nufacture of autovaccines for veterinary use referred to in paragraph 3 of Article 2 of Regulation (EU) 2019/6 of 11 December 2018 is carried out by a qualified person or a company or body employing a…
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Showing 1351–1360 of 3730 articles for “Art. EU Directive 85/374/EEC”
…nufacture of autovaccines for veterinary use referred to in paragraph 3 of Article 2 of Regulation (EU) 2019/6 of 11 December 2018 is carried out by a qualified person or a company or body employing a…
…manufacturing authorisation to have a qualified person in accordance with Article 97 of Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal…
The advertising of certain devices mentioned in Article 1 of Regulation (EU) 2017/746, the failure of which is likely to cause a serious risk to health and the list of which is set by order of the Min…
…estry tractors and their separate technical units, systems or components are subject to Regulation (EU) No 167/2013 of the European Parliament and of the Council of 5 February 2013 on type-approval an…
…sted in Article R. 5211-56, under the conditions laid down in Article 5 of Implementing Regulation (EU) No 920/2013.
…tem are replaced by references to the locally applicable social assistance scheme; 4° References to Directive 2004/38 of the European Parliament and of the Council of 29 April 2004 on the right of cit…
…tem are replaced by references to the locally applicable social assistance scheme; 4° References to Directive 2004/38 of the European Parliament and of the Council of 29 April 2004 on the right of cit…
…2° In the first paragraph of article L. 614-2, the words: "and any proposed Community regulation or directive before its examination by the Council of the European Union" as well as the words: "to the…
…2° In the first paragraph of article L. 614-2, the words: "and any proposed Community regulation or directive before its examination by the Council of the European Union" as well as the words: "to the…
…ct to substantial manipulation within the meaning of Annex I to Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products an…
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