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Showing 1521–1530 of 38109 articles for “Art. R 418-6”
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de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn…
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…
A natural or legal person who assembles devices bearing the CE marking, in accordance with their intended purpose and within the limits of use laid down by their manufacturers, in order to place them…
A custom-made device is any medical device manufactured specifically in accordance with the written prescription of a duly qualified practitioner, or any other person who is authorised to do so by vir…
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.
When advertising in favour of a veterinary pharmaceutical company or establishment mentions a veterinary medicinal product, it is governed by the provisions of Section 8 of Chapter I of this Title. Th…
The medical devices which must be notified in accordance with Article L. 5211-4 are class IIa, IIb and III medical devices and active implantable medical devices. The communication is made to the Dire…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail sends a warning to the company in question, together with the inspection report o…
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