Article R5124-48-2
When the companies and organisations mentioned in article R. 5124-2 become aware of the falsification or suspected falsification of medicinal products which they manufacture, operate or distribute, wh…
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Showing 4981–4990 of 7327 articles for “Art. 18 March 2020”
When the companies and organisations mentioned in article R. 5124-2 become aware of the falsification or suspected falsification of medicinal products which they manufacture, operate or distribute, wh…
The national vigilance system comprises : 1° The Agence nationale de sécurité du médicament et des produits de santé ; 2° The competent administrative authorities designated in accordance with the pro…
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5141-47-9 to R. 5141-47-11, the Director General of the Agence nationale de sécurité sani…
Presenting, at scientific or technical meetings, exhibitions or demonstrations, in vitro diagnostic medical devices that do not comply with the provisions of articles R. 5221-10 and R. 5221-14 without…
The health agency poison control centre provided for in article L. 6431-3 is responsible for responding, particularly in an emergency, to any request for risk assessment and any request for an opinion…
…ordance with Article L. 54-10-3, applicants must send the following information to the Autorité des marchés financiers: 1° The identity of the persons referred to in 1° and 2° of Article L. 54-10-3, d…
I.-Notwithstanding the provisions of Article R. 225-86, in companies whose shares are admitted to trading on a regulated market or to the operations of a central depository, the right to participate i…
I. - The financial futures instruments referred to in 6° of the I of article L. 214-36 and in article L. 214-38 are those referred to in 1, 5 and 6 of the I of article D. 211-1 A . II. - An undertakin…
…evant to the assessment provided for in Article R. 532-15-1. The decision taken by the Autorité des marchés financiers shall mention any opinions or reservations expressed by this competent authority.…
…fications shall be made under the conditions set out in Commission Delegated Regulation (EU) 2017/1018 of 29 June 2016 supplementing Directive 2014/65/EU of the European Parliament and of the Council…
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