Article R5141-62
…homeopathic veterinary medicinal products referred to in Article L. 5141-9, on the basis of an application accompanied by a dossier submitted and examined in accordance with the conditions laid down i…
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Showing 5811–5820 of 49021 articles for “Art. CA Paris 6-2-2023 n° 21/10189”
…homeopathic veterinary medicinal products referred to in Article L. 5141-9, on the basis of an application accompanied by a dossier submitted and examined in accordance with the conditions laid down i…
…on, de l'environnement et du travail. Registration is valid for five years. It is renewable on application by the holder to the Director General of the Agence nationale de sécurité sanitaire de l'alim…
Amendments 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…
…rmacist or veterinarian by a pharmacist or veterinarian bound by agreement with the company in this capacity. In the event of the death or permanent cessation of activity of the pharmacist or veterina…
The necessary measures are taken to prevent contamination of other food categories by medicated feed and contamination of medicated feed during manufacture, import, distribution or transport.
Medicated premixes and medicated feeds are stored in locked premises or in hermetically sealed containers separated by category and specially designed for the conservation of these products.
Authorised bodies shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn…
…manufacturers' instructions, it is considered to be a device in its own right subject to the certification procedures.
…and kits are accompanied by the information mentioned in Article R. 5211-22, including, where applicable, the information supplied by the manufacturers of the devices that have been assembled. They d…
The approved body may require the manufacturer to provide any information and to carry out any test or assessment necessary for it to carry out the verifications for which it is responsible.
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