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Évaluation des risques générée par un processus de réglementation (RA)
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last updated: 16 juin 2026
Informations générales
Risk assessment of the ProteqFlu Vaccine - Technical Opinion No. 3637/2013.
EN
16 mai 2013
Détails de l’évaluation des risques
  • Proteqflu - equine influenza vaccine
    | Merial | Production de composés médicaux ou pharmaceutiques (humains ou animaux) (Vaccins), Use as vaccine
The ProteqFlu vaccine for import, storage, transport and marketing activities. Its immunogenic agents are recombinant canarypox poxviruses, carrying the gene encoding the HA protein of the equine influenza virus, strains vCP1533 and vCP2241. The vaccine is produced by Merial in Lyon, France, and the product will be imported ready and finished. The ProteqFlu vaccine has been marketed in the European Union (approved by the European Medicines Agency) since 2003, with no relevant records of adverse events involving the GMOs in question.
EN
Méthode et points à examiner
The ProteqFlu vaccine, intended for active immunization of horses against equine influenza (H3N8) is not potentially causing adverse effects.
EN
FR
FR
The risk classification of the genetically modified organism present in the vaccine is risk class 1 (low individual risk and low risk to the community), the data presented show that this vaccine does not imply additional risks to human health, the environment and the animal production, and the post-commercial release monitoring plan is comprehensive and well structured.
EN
FR
It does not pose a risk to human, animal or environmental health.
EN
The ProteqFlu vaccine, intended for active immunization of horses against equine influenza (H3N8) is not potentially causing significant environmental degradation or harmful to human and animal health. 
EN
Molecular traditional methods. 
EN
Partage d’informations avec d’autres bases de données
Oui
Information supplémentaire
FR
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