Ministry of Health — Republic of Vanuatu
Vanuatu MoH · Vanuatu · oceania
Vanuatu's 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, with practical reliance on PIC-cooperating reference jurisdictions.
Regulatory Profile
- Agency type
- national regulator
- Region
- oceania
- Country
- Vanuatu
- Leech status
- unregulated
- Last ASH review
- 2026-05-27
- Website
- https://moh.gov.vu
Relevant Regulation Codes
- Vanuatu Pharmacy (Control) Act [Cap. 116] and amendments
- Pacific Island Countries (PIC) joint procurement arrangements through the Pacific Pharmaceutical Procurement Service where applicable
Prescriber Requirements
- Vanuatu Medical Board–registered physician — order required for any biomedical device application
- Allied health professional application under physician supervision per institutional protocol
Supply Chain & GMP
Vanuatu MoH registration as applicable; English, French and Bislama-language labelling per local convention. Standard cold-chain conditions, with logistical constraints typical of remote Pacific island distribution.
Import/Export Rules
Vanuatu MoH and Department of Biosecurity Vanuatu clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.
Reimbursement Context
Vanuatu's public health system coverage depends on inpatient bundling; 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. Pacific island nations frequently rely on Australian TGA, New Zealand Medsafe and WHO-prequalified products via Pacific cooperation arrangements; whether this captures live-organism medical devices has not been independently mapped by ASH.
Related Jurisdictions
TGA — Australia
Australia's therapeutic-goods regulator — medicinal leeches included in the Australian Register of Therapeutic Goods (ARTG) as Class IIa medical device with import permit oversight.
Medsafe — New Zealand
New Zealand's medicines and medical-devices regulator — operates under the Medicines Act 1981 with leech therapy regulated as a notified medical device and biosecurity-controlled import.
Fiji PTS — Fiji
Fiji's Pharmacy and Therapeutics Section (under the Ministry of Health and Medical Services) — leech-specific regulatory pathway has not been independently verified by ASH; medicinal leeches fall under the general national medical device framework as appropriate.
PNG NDoH-MC — Papua New Guinea
Papua New Guinea's National Department of Health, Medicines and Cosmetics Branch — leech-specific regulatory pathway has not been independently verified by ASH; medicinal leeches fall under the general national medical device framework as appropriate.