Article R1311-9
The hermetically sealed packaging of each unit consisting of the jewellery item and its support, whether placed on the market free of charge or in return for payment, shall bear the following informat…
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Showing 4321–4330 of 7195 articles for “Art. n° 18PA03648 · CAA Marseille 31 March 2023”
The hermetically sealed packaging of each unit consisting of the jewellery item and its support, whether placed on the market free of charge or in return for payment, shall bear the following informat…
Without prejudice to Article 48 of Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on the classification, labelling and packaging of substances and mixtu…
…manage AIFs for the first time under the freedom to provide services shall provide the Autorité des marchés financiers with documentation containing the following information:1° The Member State in wh…
…conomic operator has not implemented the corrective measures prescribed on the basis of Article R. 4314-11, the market surveillance authority may, on the basis of Article L. 4314-2, by order, prohibit…
The file for the reduction of a reference perimeter includes: 1° A plan showing the location of the reference perimeter including the communes remaining within whose territory the provisions of articl…
Unless there is a risk to patients' health, proprietary medicinal products which fulfil the conditions for being a reference proprietary medicinal product in an existing hybrid group may, by decision…
Unless there is a risk to patients' health, proprietary medicinal products which fulfil the conditions for being a reference proprietary medicinal product in an existing generic group may, by decision…
The marketing authorisation holder may, by written reasoned request, refer the matter to the Committee for Medicinal Products for Human Use referred to in Article 56 of Regulation (EC) No 726/2004 of…
In the absence of agreement within the coordination group, the Community arbitration procedure provided for in Articles 36 to 38 of Directive 2001/82/EC of the European Parliament and of the Council a…
The certificate accompanying medicated feedingstuffs manufactured in another Member State of the European Union or party to the Agreement on the European Economic Area when they are imported correspon…
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