Article R5141-118
Companies that produce substances mentioned in II of Article L. 234-2 of the Rural and Maritime Fishing Code, i.e. beta-agonists, oestrogens, androgens or gestagens, and those that trade in the said s…
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Showing 2141–2150 of 36450 articles for “Art. BAF 3/11 n° 106”
Companies that produce substances mentioned in II of Article L. 234-2 of the Rural and Maritime Fishing Code, i.e. beta-agonists, oestrogens, androgens or gestagens, and those that trade in the said s…
As stated in Article R. 234-7 of the French Rural and Maritime Fishing Code, which reads as follows: "The administration of veterinary medicinal products mentioned in article D. 234-6 to animals of sp…
The establishments mentioned in article L. 5142-1 which distribute veterinary medicinal products containing substances with anabolic or anticatabolic activity, in particular beta-agonists, oestrogens,…
For animals whose flesh or 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 tha…
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 Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail may request from the applicant any additional information necessary for the exami…
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…
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.
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