Draft Regulation on Procedures for the Approval of the Implementation of Preclinical Trials for Natural Medicines, Quasi-Medicines, Health Supplements, and Cosmetics: Optional PPUPK and Non-Animal Testing Pathways for Cosmetics Proposed

The Indonesian Food and Drug Authority (Badan Pengawas Obat dan Makanan– “ BPOM ”) is preparing a Draft Regulation on Procedures for the Approval of the Implementation of Preclinical Trials for Natural Medicines, Quasi-Medicines, Health Supplements, and Cosmetics (“ Draft Regulation ”). The Draft Regulation governs Preclinical Trial Implementation Approvals (Persetujuan Pelaksanaan Uji Praklinik– “ PPUPK ”). [1]