The manufacture of autovaccines for veterinary use referred to in paragraph 3 of Article 2 of Regulation (EU) 2019/6 of 11 December 2018 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.