The provisions of this section apply only to medicinal products appearing on the list established by order of the Minister for Health made on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé and after obtaining the opinion of the Director General of the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail.
The provisions of this section do not apply to medicinal products for human use or veterinary medicinal products containing micro-organisms or toxins which have been inactivated or mitigated to ensure a sufficient level of safety for public health and described in the marketing authorisation dossier, the temporary authorisation for use and the authorisation for the preparation of autovaccines for veterinary use.