CHAPTER III

PROCEDURES FOR MARKETING AUTHORISATIONS
Section 2

Marketing authorisations valid in a single Member State (‘national marketing authorisations’)

Procedure for national marketing authorisation
Article 47
1
The procedure for granting or refusing a national marketing authorisation for a veterinary medicinal product shall be completed within a maximum of 210 days of the submission of the valid application.
2
The competent authority shall prepare an assessment report containing the information referred to in Article 33.
3
The competent authority shall make the assessment report publicly available, after deleting any commercially confidential information.