This session will focus on the Veterinary Medicinal Products Regulation (NVR, Regulation 2019/6) and its practical implications. The program will include presentations from various speakers covering topics such as parallel distribution/import, pharmacovigilance, and an overview of the updated legislation and related procedures (regulatory, publicity, quality, GDP, samples, and clinical trials). The session will also address inspection and good practice, and highlight areas where the industry can further improve compliance with the new regulatory requirements.

Detailed program to follow, but you can already register!

Including welcome coffee and coffee break.