Background The regulatory requirements for approval of generic medicines and the format of compiling drug dossiers vary among regulatory authorities. The variation is particularly wide between High-income countries (HIC) and lower and middle-income countries (LMIC) with different regulatory frameworks. In this study. document requirements for approval of generic products. https://www.bekindtopets.com/top-sale-Granular-foveolae-3911-limited-choice/