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Showing 13431–13440 of 39711 articles for “Art. al. 3”
…he medicated feed extemporaneously in accordance with the good practices mentioned in article R. 5143-1. Medicated feed may only be prepared extemporaneously from a single medicated premix. However, w…
…produits de santé, specifies the conditions for applying the procedures defined in Articles R. 5211-37 to R. 5211-52.
…e manufacturer shall draw up a declaration containing the information referred to in Articles R. 1123-37 to R. 1123-41 and certifying that the medical device concerned complies with the essential requ…
…turer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking account of…
…ufacturers of medical devices or active implantable medical devices referred to in Article R. 5211-23-1, or their authorised representatives, shall define and implement a risk analysis and management…
Under the conditions laid down in article L. 5143-7, the regional prefect of the group's registered office approves the animal health programmes and grants approval to the groups mentioned in article…
The presentation, at scientific or technical meetings, exhibitions or demonstrations, of medical devices which do not comply with the provisions of this Title is authorised provided that a visible sig…
…ry, or his representative, Vice-Chairman; c) An official veterinarian mentioned in V of article L. 231-2 of the Rural and Maritime Fishing Code, appointed by the Regional Prefect; d) A pharmacist insp…
If one or more of the bodies mentioned in article D. 5143-8, consulted with a view to setting up the Commission, have not formulated a proposal within one month of receiving the request from the Regio…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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