The Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail may automatically vary a marketing authorisation for a veterinary medicinal product in order to restrict the indications, limit the conditions of supply, change the dosage, add a contraindication or any other preventive measure when it appears :
1° Either, in particular following evaluation of the data mentioned in article R. 5141-90, that the medicinal product no longer satisfies the conditions mentioned in article L. 5141-6;
2° Or that it is necessary to update it in the light of scientific knowledge, in the interests of animal health or for any other public health reason, and, where appropriate, at the request of the Minister for Agriculture or the Minister for Health;
3° or that it is necessary to bring it into line with a decision taken under the procedures mentioned in sub-section 3a of this section.