Article R5141-72
…e, the package leaflet of the homeopathic veterinary medicinal products referred to in article L. 5141-9 must bear the following information exclusively: 1° The very clear indication "homeopathic vete…
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Showing 9781–9790 of 24237 articles for “Art. al. 4”
…e, the package leaflet of the homeopathic veterinary medicinal products referred to in article L. 5141-9 must bear the following information exclusively: 1° The very clear indication "homeopathic vete…
…omeopathic veterinary medicinal product or a series of medicinal products mentioned in article L. 5141-9 is sent to the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et…
…ntrol file for each pharmaceutical form and a description of the dilution and dynamisation methods; 4° The reference of the authorisation to manufacture the medicinal products in question or a documen…
…onnement et du travail. Registration decisions include the information provided for in Article R. 5141-63.
…endments concerning the data mentioned in the application and dossier provided for in articles R. 5141-63 and R. 5141-64 are submitted for approval to the Director General of the Agence nationale de s…
…or human use administered to an animal under the conditions provided for in a of 3° of article L. 5143-4, shall immediately report it to the Agence nationale de sécurité sanitaire de l'alimentation, d…
…on of the decentralised procedure or the mutual recognition procedure provided for in articles R. 5141-47-1 et seq., any company exploiting a veterinary medicinal product authorised under one of these…
The holder of an authorisation referred to in Article L. 5141-12 must report to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail,…
The company exploiting a veterinary medicinal product may not communicate to the public information on this veterinary medicinal product relating to pharmacovigilance without transmitting it, beforeha…
…erinary medicinal products authorised by the European Medicines Agency in Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures fo…
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