Article R1423-38
The director of the registry manages the registry's staff. He allocates and assigns them to the council's departments. In the industrial tribunals mentioned in the second paragraph of article L. 123-1…
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Showing 2071–2080 of 62190 articles for “Art. R. 123-54 and R. 123-103 · C. civ. Art. 1857”
The director of the registry manages the registry's staff. He allocates and assigns them to the council's departments. In the industrial tribunals mentioned in the second paragraph of article L. 123-1…
In the event of failure to comply with the provisions of the third paragraph of Article R. 526-16 and article R. 526-22, the judge responsible for overseeing the trade and companies register in the ju…
The establishments or organisations mentioned in b of 2° of article R. 1241-31 ensure that the unique donation number that they allocate is unique on the basis of the provisions of the order and good…
…Agence nationale de sécurité du médicament et des produits de santé, pursuant to Article L. 1243-2 and the first and second paragraphs of II of L. 1245-5.II. - The unique European code is allocated a…
…e is allocated by the establishments or organisations authorised under Article L. 1243-2, the first and second paragraphs of II of Article L. 1245-5, the first paragraph of II of article L. 1245-5-1,…
…L. 123-3 and…
…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…
For the medicinal products 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 car…
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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