Article R5141-139
The labelling of self-vaccines for veterinary use and, where appropriate, the accompanying information sheet must include, in addition to the words: "self-vaccine for veterinary use" in clearly visibl…
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Showing 4221–4230 of 14294 articles for “Art. BOI-RFPI-BASE-20-20 n° 10”
The labelling of self-vaccines for veterinary use and, where appropriate, the accompanying information sheet must include, in addition to the words: "self-vaccine for veterinary use" in clearly visibl…
When the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail notifies the holder of the parallel import authorisation for a proprietary v…
The authorisation holder shall inform the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail of the date on which the activity of prepar…
After it has been issued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du…
Veterinarians providing the services referred to in Article L. 5141-15 who comply with the provisions of Article L. 241-3 of the Rural and Maritime Fishing Code may use in France veterinary medicinal…
The authorisation may be modified, suspended for a maximum period of one year or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement e…
…of the pharmacovigilance data drawn up on the basis of the reports provided for in Article R. 5141-105; 2° Depending on the case, either an updated dossier taking account of the authorised changes, o…
I.- In the event of repackaging, the holder of a parallel import authorisation for a proprietary veterinary medicinal product shall notify the holder of the marketing authorisation for the proprietary…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail may issue to veterinary pharmaceutical establishments exporting medicated feeding…
Autovaccines are prepared under the responsibility of a qualified person, who has obtained the authorisation provided for in article L. 5141-12, in facilities which may, where appropriate, be made ava…
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