Article R3213-12
…partment or a departmental public establishment, with a view to administering or liquidating the assets dependent on this legacy, shall be brought to the attention of the accounting officer. The same…
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Showing 2121–2130 of 61869 articles for “Art. R. 512-39-1 et s.”
…partment or a departmental public establishment, with a view to administering or liquidating the assets dependent on this legacy, shall be brought to the attention of the accounting officer. The same…
Any notary depositing a will containing a legacy in favour of a department or a departmental public establishment is required, as soon as the will is opened, to give notice thereof to the president of…
…me of delivery or sending into possession, the revenue or expenditure transactions affecting the assets bequeathed to a department or departmental public establishment are carried out under the contro…
Notices or documents intended for the accounting officer of the department or departmental public establishment are sent through the intermediary of the departmental or, where applicable, regional dir…
The prior declarations and supporting documents mentioned in articles R. 2213-2-2, R. 2213-5, R. 2213-7, R. 2213-8, R. 2213-8-1, R. 2213-10, R. 2213-13, R. 2213-14, R. 2213-21 and R. 2213-28 are kept…
…cted; 3° For the medicinal product undergoing the trial, the information mentioned in 4° of Article R. 5141-8 ; 4° For a reference medicinal product, the information mentioned in 5° of Article R. 5141…
…ystem, any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 : 1° Implements a risk management system for each medicinal product or each product for…
…cts mentioned in 1° of II of article L. 5121-12 and in II of article L. 5121-12-1, the obligations set out in article R. 5121-161 and articles R. 5121-166 to R. 5121-170 are carried out in accordance…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 shall implement a pharmacovigilance system in order to fulfil its pharmacovigilance obligations…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 is required to: 1° Record all adverse reactions suspected of being due to a medicinal product o…
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