Article D514-9
…the deed recording the pledge of these items. This deed shall be drawn up in writing or on another durable medium.II. - The deed formalising the agreement of the borrower and the cashier to the loan…
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Showing 1601–1610 of 28899 articles for “Art. Loi 2023-171 du 9 mars 2023”
…the deed recording the pledge of these items. This deed shall be drawn up in writing or on another durable medium.II. - The deed formalising the agreement of the borrower and the cashier to the loan…
…assets under management thus obtained with the applicable threshold set out in IV of Article L. 532-9.UCITS for which the portfolio management company acts as management company are not included in th…
…assets under management thus obtained with the applicable threshold set out in IV of Article L. 532-9.UCITS for which the portfolio management company acts as management company are not included in th…
…assets under management thus obtained with the applicable threshold set out in IV of Article L. 532-9.UCITS for which the portfolio management company acts as management company are not included in th…
…ional health data system as well as information relating to the databases that feed it; 2° The procedures for exercising the rights provided for in II and III of this article; 3° The list and characte…
…mentioning this or these activities: 1° The preparation of doses to be administered of medicinal products mentioned in article L. 4211-1 or experimental or ancillary medicinal products defined in arti…
In the event of a project to create a new commune resulting from the merger of all the member communes of one or more public establishments for inter-communal cooperation with their own tax status, th…
…5.58 € 5 Copy 1.13 € 6 Verification of costs 2.24 € 7 Litigation relating to commercial registers 8.93 € 8 Diligences linked to the expertise 16.72 € 9 Summons or notice 1.13 € 10 Visa, mark and initi…
The holder of a marketing authorisation for a medicinal product shall immediately inform the Agence nationale de sécurité du médicament et des produits de santé, specifying the reasons, of any action…
The person responsible for compliance, within the Etablissement Français du Sang, with the regulations relating to the quality and safety of blood products referred to in Article L. 1222-2 is responsi…
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