Article R5141-122-1
…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) No 1950/2006 of 13 D…
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Showing 2301–2310 of 57777 articles for “Art. n° 12-16956 and n° 12-15505”
…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) No 1950/2006 of 13 D…
…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 country of origin, which is intend…
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…
…ained marketing authorisation in France, provided that these differences have no therapeutic impact and do not entail any risk to public health.II. - The labelling of the proprietary veterinary medici…
…thorised within the meaning of Articles 44 or 65 of Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 as amended on the Community code relating to veterinary medici…
…pplication for authorisation relates to the importation of veterinary medicinal products authorised and supplied in a Member State of the European Union. The time limits mentioned in the first two par…
…l'alimentation, de l'environnement et du travail. It shall mention : 1° The name or corporate name and address of the applicant ; 2° As regards the veterinary medicinal product which has obtained mar…
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…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail shall notify the interested party of his decision with regard to the proven or po…
…by the same company or by an associated company or working under licence with the same quantitative and qualitative composition in active ingredients and excipients and the same pharmaceutical form as…
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