EthiopiaGovernment Agency Regulatory Directive
Low-Risk Traditional Medicinal Products Regulation Directive No. 1102/2025
Ethiopian Food and Drug Authority.
This directive establishes regulatory requirements for locally produced traditional medicinal products classified as low risk. It addresses product manufacturers, competency certification, production and distribution requirements, facility inspections and regulatory oversight. It aims to ensure that traditional medicinal products meet appropriate safety, quality and efficacy requirements before being marketed.
- Country
- Ethiopia
- Type
- Government Agency Regulatory Directive
- File size
- 330 KB
Sourced from official government publications. Always verify against the official source before relying on this document for legal purposes.
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