Article L451-3
…o have been fulfilled when the company has informed the market pursuant to Article 5 of Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Mark…
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Showing 2231–2240 of 2758 articles for “Art. EU Reg. 650/2012”
…o have been fulfilled when the company has informed the market pursuant to Article 5 of Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Mark…
…ot apply to limit orders for an unusually large size within the meaning of Article 4 of Regulation (EU) No 600/2014 of the European Parliament and of the Council of 15 May 2014 on markets in financial…
…stems, strategies and procedures implemented by Class 2 investment firms to comply with Regulation (EU) 2019/2033 and to identify, measure and manage the risks to which they are or may be exposed, as…
…tly assess the risks involved; 2° Subscribers or members who allocate a premium of at least 100,000 euros to the acquisition of rights expressed in these units of account; 3° Or, where the units or sh…
…for the application of this Article are set out in Article 238 of Commission Delegated Regulation (EU) 2015/35 of 10 October 2014.
…France.II. - The transaction covered by the guarantee represents an amount in excess of 10 million euros.III. - The guarantee may only be granted if it is necessary to substantially improve the condi…
Where an authority of another Member State of the European Union or party to the Agreement on the European Economic Area responsible for the prudential supervision on a consolidated basis of a group c…
…on that has been the subject of a resolution measure. Notwithstanding the provisions of Regulation (EU) 2017/1129 of 14 June 2017 and Article L. 421-14, 3° and 4° are implemented without the need to o…
…s that have been the subject of the report or notification referred to in Article 16 of Regulation (EU) No 596/2014 of the European Parliament and of the Council of 16 April 2014 on market abuse (Mark…
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…
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