Article R5121-147
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
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Showing 2831–2840 of 6073 articles for “Art. 28 March 2012”
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
…114-9 and L. 3114-10 In Title IIL. 3120-1 to L. 3122-5L. 3123-1Resulting from Law no. 2023-171 of 9 March 2023 containing various provisions adapting to European Union law in the fields of the economy…
…114-9 and L. 3114-10 In Title IIL. 3120-1 to L. 3122-5L. 3123-1Resulting from Law no. 2023-171 of 9 March 2023 containing various provisions adapting to European Union law in the fields of the economy…
I. - The operator of a trading venue shall implement quotation step regimes for shares, representative certificates, listed funds, preferential certificates and other similar financial instruments, as…
…ial instrument.II. - The manager of a trading platform shall immediately report to the Autorité des marchés financiers any significant breach of the rules of the platform, any trading condition likely…
…t instrument that has been subject to a write-down. It may request the Chairman of the Autorité des marchés financiers to take any measure necessary to apply the above provisions. For the application…
…natural or legal persons, the Autorité de contrôle prudentiel et de résolution and the Autorité des marchés financiers shall cooperate with the European Securities and Markets Authority, established b…
A pharmaceutical establishment exporting a medicinal product must ask the Agence nationale de sécurité du médicament et des produits de santé to certify that it holds the authorisation referred to in…
The following constitutes a breach subject to a financial penalty: 1° Failure by a marketing authorisation holder or a pharmaceutical company exploiting a medicinal product to constitute the safety st…
…untry, in a Member State of the European Union other than France, shall first send the Autorité des marchés financiers a notification file for each AIF concerned.II. - When units or shares of a feeder…
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