Article R5142-58
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…
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Showing 3541–3550 of 8742 articles for “Art. 9 mars 1994”
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.
…class II a medical devices or class I medical devices, the provisions laid down in Article R. 5211-49 apply subject to the following modifications: 1° For class II a medical devices, the authorised bo…
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.
…ferred to in Article R. 5211-41 or with the technical documentation referred to in Article R. 5211-39 under the conditions described in this sub-section. In addition, in the case of medical devices pl…
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…
Authorisation may only be granted if the holder has access, on site or by agreement, to medical biology tests and labile blood products within a timeframe that is compatible with the safety of treatme…
The holder of the authorisation ensures that patients are diagnosed and treated on a permanent basis, in liaison with the emergency medicine structures mentioned in article R. 6123-1, including via te…
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