CONGO

The Republic of the Congo also called Congo-Brazzaville is a country in Central Africa with a population of 5 million inhabitants, and as an official language French
Medicines and other health products such as medical devices can only be imported after registration and approval by the competent authorities.
A registration and a GMP certificate in the country of origin are also required as a prerequisite.
The Marketing Authorization granted by Congo is valid for a period of 5 years.

Medicines market in Congo
The African market in general is a high-volume import market, in Africa local production is for only 3% of world production, while the market is expanding and demand is growing. 
The introduction of noncommunicable diseases in addition to major pandemics on the continent led to a very strong demand for medicines.

Registration of medicines in Congo
Congo has its own national regulations and regulatory texts concerning the registration of medicines.
The registration file in Congo must be in CTD format and in French language.
The authority governing the registration of medicines:  Directorate of Pharmacy and Medicines, website: https://www.dpm-congo.net/
AREMA offers you a total assistance for Congo regulatory intelligence and offers you the possibility of register and market your products in Congo through a long experience of around 20 year and qualified local experts.
We thus provide you regulatory services from regulatory intelligence projects, verification, preparation and translation of your files, filing, monitoring and registration of your products until the establishment of a pharmacovigilance system,  post marketing monitoring and maintenance of the MA.

In order to initiate any collaboration or for any consultation you can contact us by email:
• info@arema-international.com