Article R5142-56
When medicated feedingstuffs 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…
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Showing 5391–5400 of 12557 articles for “Art. CJUE 30-9-2021 aff. 299/20”
When medicated feedingstuffs 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…
In establishments authorised to manufacture and import medicated feed, the following information is recorded:1° The date of manufacture, import, transfer or issue as appropriate and, if manufacture ha…
In establishments authorised to distribute medicated feed, the following information is recorded: 1° The date of acquisition, transfer or issue ; 2° The trade name or, failing that, the nature and qua…
In establishments manufacturing medicated feed, the pharmacist or veterinarian in charge or, where applicable, the pharmacist or veterinarian referred to in Article R. 5142-54 ensures that : 1° Only m…
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…
When medicated feed is supplied to a distributor or breeder in closed packaging or containers, the way in which the packaging or containers are closed prevents them from being reused after opening.
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
As part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessm…
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