Article R214-13
…to supervision equivalent to that applicable to UCITS and that cooperation between the Autorité des marchés financiers and the supervisory authority of this undertaking or fund is sufficiently guarant…
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Showing 4711–4720 of 6290 articles for “Art. 28 March 2014”
…to supervision equivalent to that applicable to UCITS and that cooperation between the Autorité des marchés financiers and the supervisory authority of this undertaking or fund is sufficiently guarant…
The liquid financial instruments referred to in 8° of I of Article L. 214-36 are :1° Treasury bills ;2° Money market instruments referred to in 2° of I of article L. 214-24-55 whose remuneration does…
In the event of adverse reactions, the Director General of Competition, Consumer Affairs and Fraud Control shall, at his request, send the Director General of the Agence nationale de sécurité sanitair…
I. - On receipt of an application for authorisation as referred to in Article L. 532-49, the Autorité de contrôle prudentiel et de résolution shall check that it is complete and, if so, shall proceed…
I -An indication of the code of conduct to which the voting consultant refers, a report on its application and, where applicable, a list of the provisions from which he has deviated, together with the…
The market surveillance authorities and authorised agents may request the economic operator concerned to provide them with : 1° The document relating to the conformity of a specimen of equipment drawn…
I.- In addition to the company's distinctive sign, the outer packaging may include signs or pictograms explaining some of the above information, as well as other information compatible with the summar…
Packages or containers of medicated feedingstuffs, including those prepared extemporaneously under the conditions provided for in articles L. 5143-2 and L. 5143-3, bear the words "medicated feedingstu…
The leaflet is drawn up in accordance with the summary of product characteristics. It includes : 1° The name or corporate name and address of the marketing authorisation holder and, where appropriate,…
For the purposes of this section, the following definitions shall apply1° Adverse reaction: a noxious and unintended response occurring at doses normally used in animals for the prophylaxis, diagnosis…
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