1.
The supervisory authorities shall have responsibility for verifying on behalf of the Community that the person responsible for placing the veterinary medicinal product on the market, or manufacturer or importer from third countries satisfies the requirements laid down in Chapter V of Directive 81/851/EEC and for exercising supervision over such persons in accordance with Chapter VI of Directive 81/851/EEC.
← Article 39 · All articles · 2. →
Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.