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Lei No 12/2017 Lei de medicamento, vacinas e outros produtos biológicos para o uso humano
This Law establishes the rules for the efficient and safe production, distribution, use and availability, as well as quality assurance of medicines, vaccines, biological and health products for citizens.
Diploma Ministerial No 223/2010 Aprova o Manual de Registo de Medicamentos
The Diploma approves the Medicines Registration Manual. The purpose of the Manual is to (a) Standardize the procedures and activities relating to the registration of medicines; (b) Clarify the doubts that professionals have encountered when interpreting the Registration Regulations; (c) Support professionals in the field in carrying out their daily activities in a standardized way; (d) Support applicants in complying with registration and post-registration procedures; (e) to make the registration process an optimized and increasingly swift process.
Diploma Ministerial no 183-A/2001 Aprova as Normas de Organização do Serviço Nacional de Saúde para o Atendimento e Tratamento de Pessoas vivendo com HIV/SIDA e os Princípios orientadores para o Tratamento de Doentes com Infecção pelo HIV/SIDA e os r...
This Ministerial Diploma approves the norms of the organization of the National Health Service for the care and treatment of people living with HIV/AIDS and the Guiding Principles for the treatment of patients with HIV/AIDS Infection and the respective Technical Guides.
Decreto No 22/99 Aprova o Regulamento de Medicamentos
This Decree regulates the production, import, marketing and dispensing of medicines and one of its objectives is to ensure that medicines in the Republic of Mozambique are safe, effective, of good quality and meet the needs of the population.