The authority is established as an autonomous body and shall be accountable to the ministry of health. It shall be seen to ensure the safety, efficacy, quality, and proper use of food and medicines. It shall also see to the ethics of practitioners and professionals, as well as facilitating the standardization of health institutions, among others.

These regulations are for the amendment of the development bank of Ethiopia’s re-establishment council of ministers regulations number 83 of 2003. This amendment covers article 7 of the previous regulation which amends the authorized capital of the bank.

These regulations are for the establishment of the forest ranger service. The service oversees and coordinates all affairs related to the protection of forests and the implementation of relevant forestry laws. It contains the powers and duties of the forest rangers, uniforms and arms, as well as appropriate panels.

These regulations are issued by the council of ministers and dissolves the tea development and marketing enterprise established by the council of ministers in 1993. The regulation also transfers all rights and obligations of the dissolved enterprise to 3 other tea development and marketing enterprises.

These regulations are to establish the food, beverage and pharmaceutical development institute as an autonomous federal government institution, and to be supervised and accountable to the ministry of industry. The institute is charged with ensuring the improvement in competitive levels of the food, beverage, and pharmaceutical industry at international levels. It contains the powers and duties, and organizational structure among others.

These regulations address the designation of the Bale national park. It is under the relevant sections and articles under the development, conservation, and utilization of wildlife regulation. It highlights chiefly, the location of the park, and its boundaries along several demarcation points referred to as beacons. It also discusses the administration of the park, its powers and duties, prohibited activities, and penalties, among other key pointers.

This directive applies to unintended releases of modified organisms, and other related incidents during the accident. It expressly states all emergency measures to be carried out in the case of a release, as well as the duties and powers of all relevant stakeholders.

These regulations address the designation of the Alitash national park. It is under the relevant sections and articles under the development, conservation, and utilization of wildlife regulations. It highlights chiefly, the location of the park, and its boundaries along several demarcation points referred to as beacons. It also discusses the administration of the park, its powers and duties, prohibited activities, and penalties, among other key pointers.

This adaptation plan seeks to build on the green economy strategy and the GTP II frameworks. It focuses on developing a resilient and sustainable green economy by prioritising selected vulnerable sectors of the economy.

The municipal public health rules are issued concerning water. It highlights several rules to this effect on the water for public consumption, human excrements, and discharge of sewage.

The directive acknowledges the need for a holistic risk assessment procedure to proceed with all transactions related to modified organisms. This is in a bid to standardize the entire procedure across the country. It defines key terms, discusses transactions subject to the directive, and expressly states the directives, among others.

This amendment deems it necessary to alter the existing raw hides and skins marketing proclamation of 2013. It seeks to solve the problems associated with quality and collection by the inclusion of skin collectors among the present actors in the market. This is to ensure the maximization of economic benefits accruable to the country and the market players

The authority is established as an autonomous body and shall be accountable to the mayor of the city of Addis Ababa. It shall be seen to ensure the safety, efficacy, quality, and proper use of food and medicines in the city. It shall also see to the ethics of practitioners and professionals, as well as facilitating the standardization of the city’s health institutions, among others.

The proclamation on food and medicine administration guides the establishment of the necessary frameworks and regulatory schemes to ensure the safety of citizens against harmful and unsafe food, drugs, narcotics, and cosmetic products.

These regulations are under Article 5 of the Definition of Powers and Duties of the Executive Organs of the Federal Democratic Republic of Ethiopia Proclamation of 1995 (as amended), and Article 64 of the Value Added Tax Proclamation of 2002.

This industrial roadmap document contains an overview of the industrial sector. It offers strategies and frameworks needed to move the industrial sector forward in line with the GTP goals of 2035.

The PASDEP acknowledges the various constraints faced by the Ethiopian economy as a result of poor policy coordination and dwindling levels of investment. The plan, therefore, seeks to facilitate the development of agriculture along the lines of human capacity development, input supply, technology adoption, and infrastructure provision.

The extension package highlights the causes of these nutrition issues and pushes to address them to achieve the prevention of diseases arising from malnutrition. The prevalence of malnourishment among the rural population in Ethiopia is well documented. This is despite the wide variety of agricultural products produced in the country.

Recognizing the levels of HIV infection across the country, these guidelines inform the implementation of Ethiopia’s national Anti-retroviral program.

These regulations are issued by the council of ministers. It addresses the issues surrounding effective food, medicine, and health care administration and control in Ethiopia. It specifically includes prominent areas like manufacturing, counterfeiting and adulteration, irradiation, transport, storage and distribution, import and export, as well as clinical trials, among others. it ultimately pushes to ensure that food and medicine unsafe for public use and consumption, do not find themselves involved in the value chain, from production to distribution, and final use.