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Showing 4261–4270 of 10563 articles for “Art. CE 27-9-2006 n° 285279”
The provisions relating to full-time practice and replacement contained in articles R. 5142-20 and R. 5142-22 to R. 5142-30 do not apply to the pharmacist or veterinarian mentioned in article R. 5142-…
The information referred to in articles R. 5142-57 and R. 5142-58 is, immediately after each operation, recorded by an appropriate system allowing immediate printing at the request of the control auth…
…ulatory provisions relating to medicated feedingstuffs is bound by an agreement with the company concerned and has at least the following duties: 1° Responsible for the quality of medicated feedingstu…
…edingstuffs are manufactured for the purposes of a clinical trial, they are manufactured in accordance with the sponsor's instructions. The person responsible referred to in article R. 5142-55 ensures…
…e and, if manufacture has been subcontracted, the date of the manufacturing order and the date of receipt of the batch;2° The name, quantity and batch number of the medicinal premix or premixes used;3…
…o issued the prescription; 6° The name and address of the breeder or animal keeper or distributor receiving the medicated feed.
…ixes covered by a marketing authorisation or a temporary authorisation for use are used, in accordance with the conditions described in this authorisation; 2° The medicated feed is manufactured from o…
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.
Within the framework of the EC declaration of conformity procedure, product quality assurance, for class II a medical devices or class I medical devices, the provisions laid down in Article R. 5211-49…
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