Article R5141-113
…products are intended for human consumption, no more than one month's treatment may be given in medicated feed. The veterinarian prescribing a medicated feed must ensure that the medicated feed prescr…
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Showing 3571–3580 of 9424 articles for “Art. CA Versailles 14-11-1996”
…products are intended for human consumption, no more than one month's treatment may be given in medicated feed. The veterinarian prescribing a medicated feed must ensure that the medicated feed prescr…
I.-Without prejudice to the provisions applicable to medicinal products classified as narcotics, any prescription for medicinal products mentioned in article L. 5143-5, as well as in II of article L.…
…ammatory, analgesic, neuroleptic, anaesthetic, hormonal or anabolic properties are subject, in application of the last paragraph of article L. 5144-1, to the specific conditions of supply defined belo…
The poison control centres referred to in article L. 6141-4 and the regional pharmacovigilance centres referred to in article R. 5121-167 shall transmit, without delay, to the Agence nationale de sécu…
…the name and address of the pharmacy or the professional domicile where the veterinary practice is carried out. The data they contain must appear on a medium which guarantees their permanence and int…
…de sécurité sanitaire de l'alimentation, de l'environnement et du travail may request from the applicant any additional information necessary for the examination of the application. In this case, the…
In the event of a dispute over the application of the classification rules between the manufacturer of a device and an authorised body involved in the certification procedures provided for in this Tit…
All manufacturers of in vitro diagnostic medical devices, or their representatives, shall appoint a person to be responsible for reactovigilance, whose identity and position shall be communicated to t…
In an emergency, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may suspend the authorisation of an advertisement for a maximum period of three months.
The CE marking may be affixed to an in vitro diagnostic medical device only if it complies with the essential requirements and has undergone the assessment procedures applicable to it. Where an in vit…
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