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The Ministry of Health together with its partners realizes that efficient and effective
delivery of...
The Government of the Republic of Zambia has placed priority on ensuring that Zambians are healt...
Qualitative study from Zambia on barriers to and facilitators of life-long learning
The Government of Republic of Zambia reported the first confirmed cases of COVID-19 on 18th Marc...
The Government of Republic of Zambia reported the first confirmed cases of COVID-19 on 18th Marc...
The attainment of Zambia’s goal of being a prosperous and middle-income country by 2030 as sti...
This document has been developed as a guide to allinstitutions producing health care waste in planning and implementation of interventions that will reduce mismanagement ... hazardous waste in Zambia.The National Health-Care Waste Management Plan for 2015 to 2019 provides an overview of the situation analysis, the proposed activities and the health care facility waste generating processes in Zambia and presents options for minimizing health-care waste generation through source reduction. The hazardous wastes generated by health care facilities are a challenge in Zambia as handling, storage, transportation and final disposal leaves much to be desired.
Phiri et al. Human Resources for Health (2017) 15:40
DOI 10.1186/s12960-017-0214-3
Biennial Report. SUBMITTED TO THE UNITED NATIONS GENERAL ASSEMBLY SPECIAL SESSION ON HIV AND AIDS
Reporting period: January 2012 – December 2013
The study on refugee economies shows that refugees and former refugees are contributing positively to Zambia’s economy in various ways and have t...
Accessed June 17,2019
Medicines and Allied Substances [No. 3 of 2013 47 | An Act to continue the existence of the Pharmaceutical Regulatory Authority ... re-name it as the Zambia Medicines Regulatory Authority; provide for the functions and powers of the Authority; provide for the registration and regulation of pharmacies, health shops and agro-veterinary shops; provide for the registration and regulation of medicines and allied substances; provide for the regulation of the manufacture, importation, exportation, possession, storage, distribution, supply, promotion, advertising, sale and use of medicines and allied substances; provide for the regulation and control of clinical trials; repeal and replace the Pharmaceutical Act, 2004; and provide for matters connected with, or incidental to, the foregoing.
