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Medicines Regulatory capacity building in the Republic of Congo

To foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public health, the Ministry in charge of health of the Republic of Congo has initiated a plan to strengthen the regulatory capacity of its Department of Pharmacy and Medicines implemented by its director, Dr Boniface OKOUYA. This process is based on a strong commitment to pharmaceutical reform for which the law will be promulgated shortly. It is in this momentum that the Directorate of Pharmacy and Medicines in partnership with the World Health Organization (WHO) and the Africlinique project, a regulatory capacity building project in Central Africa (funded by the European Union  through EDCTP), will carry out a self-assessment of its pharmaceutical regulatory system using the Global Benchmarking  Tool (GBT) developed by the WHO, which also focuses on clinical trials oversight.

By Dario Scaramuzzi

Pro-bono Partnership & Capacity Development Manager at R-Evolution Worldwide

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