Article R6333-12-1
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…
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Showing 3361–3370 of 8984 articles for “Art. n° 22-18436 · AFNOR NF K 12-500”
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…
The skills operator authorised in application of article R. 6523-2-10 specifies in an appendix to the statistical and financial statement provided for in article R. 6332-31, for the territory, the amo…
…n the Director General of the Agence nationale de sécurité du médicament et des produits de santé makes a reasoned request, the person responsible for placing the product on the market shall send him…
…e de l'alimentation, de l'environnement et du travail shall grant, vary, suspend or withdraw the marketing authorisation within a period of thirty days, in accordance with the decision taken by the Eu…
In the event of infringement of the applicable legislative and regulatory provisions, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may suspend or wit…
…ne 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 to Commission Regulation (EC)…
…sing :1° For each presentation, a sample of the proprietary medicinal product which has obtained marketing authorisation in France and a sample of the proprietary medicinal product marketed in the cou…
By way of derogation from article R. 5141-123, the importation of veterinary medicinal products intended exclusively for animals whose flesh or products are not intended for human consumption is not s…
…t authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provided that these differences have no therapeutic impact and do no…
…mmary of product characteristics, the conditions of prescription, supply and administration, the package leaflet and the labelling of the proprietary veterinary medicinal product as it will be markete…
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