I.-The manufacture, import, export and wholesale distribution of veterinary medicinal products, and the manufacture, import and distribution of medicinal products subject to clinical trials, are carried out by establishments governed by Regulation (EU) 2019/6 of 11 December 2018 and by this chapter.
II.-In each establishment authorised under Article 88 of Regulation (EU) 2019/6 of 11 December 2018, a qualified person is responsible in particular for carrying out the tasks specified in Article 97 of the same Regulation.
III.-In each wholesale distribution establishment for veterinary medicinal products authorised under Article 99 of Regulation (EU) 2019/6 of 11 December 2018, one person is responsible for carrying out the tasks specified in Article 101 of the same Regulation.
IV. -The persons referred to in II and III shall be personally responsible for compliance with the provisions of points 6 to 8 of Article 97 and the provisions of Article 101 of Regulation (EU) 2019/6 of 11 December 2018 and of this Book relating to their activity, respectively, without prejudice, where applicable, to the joint and several liability of the company.