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Showing 4171–4180 of 56695 articles for “Art. comité juridique of 9 January 2019”
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…
…horised 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 has been subcontracted,…
…shments 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 quantity of t…
…orisation; 2° The medicated feed is manufactured from only one medicated premix, with the exception of medicated feeds manufactured, when the veterinary surgeon's prescription expressly so provides, f…
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.
…in hermetically sealed containers separated by category and specially designed for the conservation of these products.
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.
…dical biology tests and labile blood products within a timeframe that is compatible with the safety of treatment.
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…
Authorisation for interventional activity under medical imaging in neuroradiology, category A, may only be granted if the holder has access to a neurosurgery unit, where applicable by agreement. Autho…
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