Article L521-7
If it is established that products do not comply with the regulations in force or present or are likely to present a danger to public health or consumer safety, the administrative authority may order…
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Showing 3931–3940 of 6290 articles for “Art. 28 March 2014”
If it is established that products do not comply with the regulations in force or present or are likely to present a danger to public health or consumer safety, the administrative authority may order…
The holder of a marketing authorisation for a medicinal product shall immediately inform the Agence nationale de sécurité du médicament et des produits de santé, specifying the reasons, of any action…
Without prejudice to any criminal proceedings that may be brought, where a product or group of products referred to in Article L. 5311-1 is placed on the market, put into service or used without havin…
In the cases referred to in Articles L. 5312-1 and L. 5312-2, and in the event of suspension or withdrawal of authorisation or registration of a product or group of products referred to in Article L.…
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…
…ing of plant protection products on the market; 2° Biocidal products covered by Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available…
…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…
Where an economic 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…
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…
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