Strengthened Stakeholder Cooperation Needed to Combat Illegal Drug Trafficking
Strengthened Stakeholder Cooperation Needed to Combat Illegal Drug Trafficking It has been emphasized that the cooperation and participation of stakeholders…
The Ethiopian Food and Drug Administration (EFDA) is mandated, in the proclamation 661/2009, to ensure the safety, quality and efficacy of medicines. To achieve this, the authority has been working on different regulatory activities. The medicine market authorization system is one of the top priority areas that have been implemented. In addition to the dedicated assessors, the authority uses a national drug advisory committee for the assessment and registration of medicines. This has evolved over the years to improve the medicine dossier evaluation system.
EFDA is the National Regulatory Body of Ethiopia which is under the Ministry of Health. The Authority is responsible to ensure the quality, safety and/or efficacy of medicines, food, cosmetics and medical devices.
EFDA was established under the Ethiopian Food and Drug Administration establishment council of Ministers Regulation No. 189/2010. After repealing the drug administration and control proclamation 176/1999, EFDA became operational as of July 17, 2010. Its budget is from the Ethiopian government. It is mandated by the Food, Medicines and Health care Administration and Control Proclamation 661/2009.
To protect the health of consumers by ensuring:-
To promote and protect the public health by ensuring safety, efficacy and quality of health and health-related products and services through product quality assessment and registration; licensing and inspection of health professionals, health institutions, pharmaceutical and food establishments, and provision of up-to-date regulatory information while promoting proper use of health and health-related products and services including proper use of medicines.
Key Features
i-Register
i-Import
i-License
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