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Chapter II · MARKETING AUTHORISATIONS – GENERAL PROVISIONS AND RULES ON APPLICATIONS  ›  Section 5 · Specific requirements for generic, hybrid and combination veterinary medicinal products and for applications based on informed consent and bibliographic data › Article 22

Application based on bibliographic data

1.   By way of derogation from point (b) of Article 8(1), the applicant shall not be required to provide the documentation on safety and efficacy if that applicant demonstrates that the active substances of the veterinary medicinal product have been in well-established veterinary use within the Union for at least 10 years, that their efficacy is documented and that they provide an acceptable level of safety.

2.   The application shall satisfy the requirements set out in Annex II.

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