Article L611-3-1
…st drawn up by the Minister, approve by decree the codes of conduct that they have drawn up for the marketing of financial instruments referred to in Article L. 211-1, banking transactions mentioned i…
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Showing 8961–8970 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
…st drawn up by the Minister, approve by decree the codes of conduct that they have drawn up for the marketing of financial instruments referred to in Article L. 211-1, banking transactions mentioned i…
…the Extraordinary General Meeting. In companies whose shares are admitted to trading on a regulated market, the number of shares eligible for this dividend bonus may not exceed 0.5% of the company's s…
…1, the abuse by an undertaking or group of undertakings of a dominant position within the internal market or a substantial part thereof is prohibited. These abuses may in particular consist of refusa…
Only medicinal products for which the marketing authorisation referred to in article L. 5121-8 or the authorisation referred to in article L. 5121-9-1 or one of the registrations referred to in articl…
…tising approval".This authorisation is issued for a period which may not exceed the duration of the marketing authorisation for medicinal products subject to this authorisation.In the event of failure…
The database of direct marketers is maintained by the Banque de France on behalf of the authorities referred to in Article L. 341-7 . The procedures for managing the file and the relations between the…
…ts for implementing the programme; 5° The number of patients concerned, as estimated by the company marketing the medicinal product; 6° The follow-up report referred to in article R. 1161-25, in the e…
…at is microbiologically sound and protected against the risks of pollution. On emergence and during marketing, it respects or satisfies the quality limits or references, relating to microbiological an…
…for each medicinal product, its name, strength and pharmaceutical form, as well as the name of the marketing authorisation holder and, if different from the latter, the name of the company or organis…
…5121-12-1 is to ensure the safety of prescribing a medicinal product which does not comply with its marketing authorisation, in order to meet the special needs of the patients concerned. It may be est…
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