Американское общество гирудотерапии

National Drug Authority — Uganda

NDA Uganda · Uganda · africa

Regulatory jurisdiction profileJurisdictional reference
Unregulatednational regulator

Uganda's National Drug Authority — leech-specific regulatory pathway has not been independently verified by ASH; medicinal leeches fall under the general national medical device framework or traditional-medicine pathways as appropriate.

Regulatory Profile

Agency type
national regulator
Region
africa
Country
Uganda
Leech status
unregulated
Last ASH review
2026-05-26

Relevant Regulation Codes

  • Ugandan National Drug Policy and Authority Act, Cap 206
  • Ugandan Traditional and Complementary Medicine Act, 2019

Prescriber Requirements

  • Uganda Medical and Dental Practitioners Council–registered physician — order required for any biomedical device application
  • Traditional and complementary medicine practitioners registered under the Traditional and Complementary Medicine Council may have separate scope; specific hirudotherapy authorisation not independently verified by ASH

Supply Chain & GMP

NDA registration as applicable; English-language labelling. Standard cold-chain conditions.

Import/Export Rules

NDA import authorisation; Ministry of Agriculture, Animal Industry and Fisheries 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. The 2019 Traditional and Complementary Medicine Act offers a possible statutory entry point for hirudotherapy under traditional-practice oversight; this has not been independently confirmed by ASH.

Related Jurisdictions

Этот сайт предоставляет образовательную информацию и не является медицинской консультацией, диагнозом или рекомендацией по лечению. Гирудотерапия сопряжена с клинически значимыми рисками и должна проводиться только квалифицированными клиницистами в рамках институционально утверждённых протоколов. Разрешение FDA 510(k) для медицинских пиявок ограничено определёнными показаниями; обсуждения исследовательского и нелицензионного применения отмечены соответствующим образом. Для индивидуальных медицинских рекомендаций обратитесь к квалифицированному медицинскому специалисту.