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Showing 4991–5000 of 16885 articles for “Art. CA Paris 29-6-2007 n° 05/17124”
…onnement et du travail shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé of his decision within fifteen days when the authorisation concerns…
…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de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn…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.
Where an authorized body finds that the requirements of this Title applicable to this device have not been met or are no longer being met by the manufacturer, or where a certificate should not have be…
…it and provided users with information containing the relevant manufacturers' instructions; 3° have carried out all these operations using appropriate methods. This declaration is kept at the disposal…
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