American Society of Hirudotherapy

Drug Regulatory Authority — Kingdom of Bhutan

Bhutan DRA · Bhutan · asia pacific

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Bhutan's national drug regulator — leech-specific authorisation pathway not independently verified by ASH.

Regulatory Profile

Agency type
national regulator
Region
asia pacific
Country
Bhutan
Leech status
unregulated
Last ASH review
2026-05-28

Relevant Regulation Codes

  • Bhutan Medicines Act 2003 and amendments
  • Bhutan Medicines Rules and Regulations 2012

Prescriber Requirements

  • Bhutan Medical and Health Council–registered physician — order required for any biomedical device application
  • Allied health professional application under physician supervision per institutional protocol

Supply Chain & GMP

Bhutan DRA registration as applicable; Dzongkha and English-language labelling. Standard cold-chain conditions, with logistical constraints typical of Himalayan distribution.

Import/Export Rules

Bhutan DRA and Bhutan Agriculture and Food Regulatory Authority (BAFRA) clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.

Reimbursement Context

Bhutan's National Health Service (free at point of care) coverage depends on inpatient bundling under Gross National Happiness Index–aligned policy.

ASH Editorial Notes

Leech-specific authorisation pathway not independently verified by ASH; falls under general medical-device / Sowa-Rigpa traditional-medicine framework as appropriate. Bhutan integrates traditional Bhutanese medicine (gSo-ba Rig-pa) into its national health service — whether this captures medicinal leech application has not been independently mapped by ASH.

Related Jurisdictions

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.