The Quality Directorate of the National Agency for Pharmaceutical Products oversees the implementation and continuous improvement of the Agency's quality management system, in line with World Health Organization standards and the maturity level 3 (ML3) regulatory pathway.
It coordinates the standardisation of registration, approval, control and inspection procedures, the continuous training of teams and the monitoring of regulatory performance indicators.
The detailed content of this section (indicators, quality standards, self-assessment reports) will be expanded in a future phase of the website.
Page updated on