Article R214-214-4
When the composition of the supervisory board of a company investment fund and the procedures for appointing its members are set under the conditions provided for in the second paragraph of I of Artic…
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Showing 3671–3680 of 69357 articles for “Art. 4°-a and 4°-c”
When the composition of the supervisory board of a company investment fund and the procedures for appointing its members are set under the conditions provided for in the second paragraph of I of Artic…
For the operations referred to in 2° and 3° of Article L. 310-1, the State in which the risk is situated is considered to be :1° The State in which the property is located, when the insurance relates…
…by the supervisory ministers. In particular, it has the following powers: 1° It approves the budget and its amendments, the financial account for the financial year ended and the allocation of the res…
…ing the practice, management or monitoring of the activity of medical electroradiology manipulators and medical laboratory technicians, the competent departments of the State and the public establishm…
…ions set out in paragraph 36 of Article 3 of Regulation (EU) No 910/2014 of the European Parliament and of the Council of 23 July 2014 on electronic identification and trust services for electronic tr…
…apply to the persons mentioned in III of Article L. 812-2 with the exception of articles R. 814-38 and R. 814-41, including where they have been authorised to continue one or more cases in progress a…
…sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines and Health Products) when the latter carry out their activity on national territory, or registered w…
Manufacturers of medicinal products must be able to document the measures they have taken to ensure that their supplier of excipients complies with good practice under the conditions set out in articl…
…cts of major therapeutic interest referred to in article L. 5111-4, marketing authorisation holders and pharmaceutical companies exploiting medicinal products shall, under their responsibility, draw u…
…as the impossibility of manufacturing or using a medicinal product. Marketing authorisation holders and pharmaceutical companies operating a medicinal product of major therapeutic interest referred to…
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