Bahagian Pengawalan Farmaseutikal — Jabatan Perkhidmatan Farmasi
Brunei DPS · Brunei Darussalam · asia pacific
Brunei's Pharmaceutical Services Department (Ministry of Health) — leech-specific regulatory pathway has not been independently verified by ASH; medicinal leeches fall under the general national pharmaceutical and medical device framework as appropriate.
Regulatory Profile
- Agency type
- national regulator
- Region
- asia pacific
- Country
- Brunei Darussalam
- Leech status
- unregulated
- Last ASH review
- 2026-05-27
- Website
- https://www.moh.gov.bn
Relevant Regulation Codes
- Brunei Medicines Order, 2007 and Medicines (Advertisement) Regulations, 2007
- Brunei national medical device regulatory framework
- ASEAN Medical Device Directive (AMDD) harmonised frameworks where applicable
Prescriber Requirements
- Brunei Medical Board–registered physician — order required for any biomedical device application
- Allied health professional application under physician supervision per institutional protocol
Supply Chain & GMP
Brunei DPS registration as applicable; Malay (Bahasa Melayu) and English-language labelling. Standard cold-chain conditions.
Import/Export Rules
Brunei DPS and Department of Agriculture and Agrifood clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.
Reimbursement Context
Brunei's universal government-financed health system covers most inpatient interventions; outpatient hirudotherapy is generally not separately reimbursed.
ASH Editorial Notes
Leech-specific pathway not independently verified by ASH; falls under general medical device / traditional medicine framework as appropriate. South-East Asian regulatory frameworks are progressively coordinating through the ASEAN Medical Device Directive (AMDD); whether this captures live-organism medical devices has not been independently mapped by ASH.
Related Jurisdictions
PMDA — Japan
Japan's medicines and devices regulator — leech therapy classified within the Kampo / traditional-medicine framework under MHLW oversight, with no PMDA-issued device approval to date.
NMPA — China
China's medical-products regulator — leeches (水蛭 / shui zhi) are codified in the Chinese Pharmacopoeia as Traditional Chinese Medicine (TCM) and regulated as a Chinese herbal medicine.
MFDS — South Korea
South Korea's drug-safety regulator (formerly KFDA) — leech therapy practised within the Korean Medicine (한의학 / Hanui) tradition; Hirudo medicinalis listed in the Korean Pharmacopoeia.
CDSCO — India
India's central drug regulator — leech therapy (Jalaukavacharana / जलौकावचारण) integrated into the official AYUSH system as part of Ayurveda Panchakarma practice.