The preparation of veterinary medicinal products not falling within the scope of Regulation (EU) 2019/6 of 11 December 2018, excluding extemporaneous preparations, is carried out by a qualified person or a company or body employing a qualified person who has obtained an authorisation for this purpose issued by the National Agency for Food, Environmental and Occupational Health Safety.
This activity is subject to pharmacovigilance obligations, the content of which is laid down by decree.
It is carried out in compliance with good practice, the principles of which are laid down by decision of the Director General of the Agence nationale chargée de la sécurité sanitaire de l’alimentation, de l’environnement et du travail.