Article R5121-76-12
…du médicament et des produits de santé or on expiry of the period provided for in II of Article R. 5121-76-11, the Minister for Defence may grant the authorisation for use provided for in Article R. 5…
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Showing 2271–2280 of 45413 articles for “Art. 12 al. 2”
…du médicament et des produits de santé or on expiry of the period provided for in II of Article R. 5121-76-11, the Minister for Defence may grant the authorisation for use provided for in Article R. 5…
…he list drawn up by the Commission of the European Communities pursuant to Article 16f of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code re…
The State is represented in court both as plaintiff and defendant by the Director General of the Caisse des dépôts et consignations for all acts relating to the management of the fund mentioned in the…
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5141-47-9 to R. 5141-47-11, the Director General of the Agence nationale de sécurité sani…
…for human use classified in one of the categories subject to restricted prescription by Article R. 5121-77, benefiting from a marketing authorisation and containing the substances listed in the Annex…
…forty-five days from the date of receipt of the complete application referred to in Article R. 5141-123-3. The period mentioned in the previous paragraph is reduced to twenty days if the application f…
The copy of the import authorisation or temporary use authorisation referred to in article L. 5141-10 is presented during the inspection by the customs officers. For imported veterinary medicinal prod…
…thin sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is reduced to thirty days for applications su…
…omplied with, in particular those relating to possession and supply referred to in Article R. 5141-112, labelling referred to in Articles R. 5141-73 to R. 5141-75, and the package leaflet referred to…
…veterinarian registers the medicinal products referred to in the first paragraph of article R. 5141-126 using any recording system that allows immediate presentation at the request of the control auth…
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