American Society of Hirudotherapy

Agence du Médicament de Madagascar

AGMED · Madagascar · africa

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Madagascar's Agence du Médicament — 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
africa
Country
Madagascar
Leech status
unregulated
Last ASH review
2026-05-26

Relevant Regulation Codes

  • Malagasy Code de la Santé — pharmaceutical and device provisions
  • Malagasy national medical device regulatory framework

Prescriber Requirements

  • Ordre des Médecins de Madagascar–registered physician — order required for any biomedical device application
  • Allied health professional application under physician supervision per institutional protocol

Supply Chain & GMP

AGMED registration as applicable; French and Malagasy-language labelling. Standard cold-chain conditions, with logistical constraints typical for island distribution.

Import/Export Rules

AGMED and Ministry of Public Health import authorisation; veterinary services clearance for live invertebrates; CITES Appendix II paperwork for Hirudo medicinalis / verbana.

Reimbursement Context

Not covered under public insurance schemes for leech therapy specifically.

ASH Editorial Notes

Leech-specific pathway not independently verified by ASH; falls under general medical device / traditional medicine framework as appropriate. Madagascar has rich traditional medicine practice; whether hirudotherapy is recognised under any statutory framework 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.