American Society of Hirudotherapy

Ministry of Health and Prevention

MOHAP · United Arab Emirates · middle east

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

UAE Ministry of Health and Prevention — federal authority over health products; leech-specific regulation has not been independently verified by ASH.

Regulatory Profile

Agency type
national regulator
Region
middle east
Country
United Arab Emirates
Leech status
unregulated
Last ASH review
2026-05-25

Relevant Regulation Codes

  • UAE Federal Law on Pharmaceutical Profession and Establishments
  • UAE national medical-device registration framework

Prescriber Requirements

  • MOHAP- / DoH-Abu Dhabi- / DHA-Dubai-licensed physician prescription required
  • Traditional and complementary medicine (TCAM) practitioner licensing varies by emirate; specific hirudotherapy authorisation not independently verified by ASH

Supply Chain & GMP

MOHAP product registration; bilingual Arabic / English labelling.

Import/Export Rules

MOHAP import licence plus Ministry of Climate Change and Environment veterinary clearance for live invertebrates; CITES Appendix II paperwork.

Reimbursement Context

Thiqa, ENAYA, Daman, and private insurance coverage for hirudotherapy not independently verified by ASH.

ASH Editorial Notes

UAE health regulation is split federally (MOHAP) and at emirate level (DoH-Abu Dhabi, DHA-Dubai). Specific leech regulatory pathway has not been independently verified by ASH. UAE has expanding traditional and complementary medicine licensing including for hijama (cupping); whether hirudotherapy is similarly licensed has not been confirmed.

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.