Draft BPOM Regulation to Allow PBF to Execute Drug Exports Through Notarized Power of Attorney; Public Input Open until 31 July 2026

The Indonesian Food and Drug Authority (Badan Pengawas Obat dan Makanan– “ BPOM ”) is currently completing work on the new Draft Regulation on Procedures for the Issuance of Drug Export Documents (“ Draft Regulation ”). In essence, the Draft Regulation specifically addresses the issuance of Certificates of Pharmaceutical Products (“ CPP ”) and Good Manufacturing Practice Compliance Certificates (“ GMP Compliance Certificates ”) by BPOM as export-related documentation for drugs. [1]