Guidelines on the Publishing of Package Insert and Patient Information Leaflet of Registered Drug Products in the Food and Drug Administration (FDA) Verification Portal System; (3 page(s), in English)

Regulations, No.: DFAR/HMDAR/TRG/002 Rev_2, Governing Registration of Medical Devices including In Vitro Diagnostics; (13 page(s), in English)

Guidelines on the Publishing of Package Insert and Patient Information Leaflet of Registered Drug Products in the Food and Drug Administration (FDA) Verification Portal System; (3 page(s), in English)