Rozporządzenie Ministra Zdrowia z dnia 21 listopada 2012 r. w sprawie Centralnej Ewidencji Badań Klinicznych w zakresie badanych produktów leczniczych weterynaryjnych

This regulation establishes and manages a central register for clinical trials involving veterinary medicinal products in Poland. It ensures that all research on animal medicines is properly documented and tracked by health authorities to maintain safety and transparency in veterinary medicine. This affects veterinary researchers, pharmaceutical companies, and clinical trial organizers who must report their studies to the central registry.