Article R4332-4
…aw no. 83-8 of 7 January 1983 on the division of powers between the communes, départements, regions and the State, the operating cost of training hours and staff costs, the remuneration of trainees an…
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Showing 3051–3060 of 62249 articles for “Art. R. 223-20 and R. 223-22”
…aw no. 83-8 of 7 January 1983 on the division of powers between the communes, départements, regions and the State, the operating cost of training hours and staff costs, the remuneration of trainees an…
In 1994, the allocation mentioned in article R. 4332-3 is distributed between the regions according to the following three criteria: a) 80%, in proportion to the expenditure incurred by the State in 1…
Pharmaceutical establishments and establishments authorised under articles L. 4211-9-1 and L. 4211-9-2 may procure tissues, their derivatives and cells from the human body, whatever their level of pro…
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,…
…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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