Article R5141-129
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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Showing 581–590 of 17465 articles for “Art. Form 2044 spéciale”
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…
After the authorisation provided for in Article L. 5141-12 has been issued, the preparation methods and control techniques mentioned in a, c and d of the technical dossier provided for in 3° of II of…
…shall certify that the declaration has been provided and shall, at his request, communicate this information to the competent authority of the importing State. The Director General of the Agency shal…
…lities, where applicable; 4° The list of pathogens by species of destination and the pharmaceutical forms envisaged. II - The application must be accompanied by a dossier containing : 1° Documents pro…
Within the meaning of article L. 5141-2, the veterinarian may only prescribe an auto-vaccine for veterinary use under the conditions of 4° of article L. 5143-4, prepared from a pathogen which he himse…
…a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse reaction, wi…
The authorisation provided for in Article L. 5141-10 is issued by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail.
…ing self-vaccines for veterinary use consists of the authorisation holder recording the following information in chronological order: 1° The name and address of the owner of the animal or farm from wh…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail will notify the applicant of his decision within one hundred and twenty days from…
…e address of the preparation site. It specifies the pathogens by target species, the pharmaceutical forms and the authorised adjuvants.
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