THE REGULATORY COMPLEXITY OF THE PHARMACEUTICAL SECTOR IN THE DRC

The regulation of medicinal products and medical consumables is a large chain, requiring not only high values, but also effective resources for its implementation to ensure rational management and quality assurance. Its study is of vital importance in human, pharmaceutical and veterinary medicine, since medicinal products are the main weapon available to paramedics and veterinary surgeons to prevent, treat, cure or relieve the sick. The reader will quickly realize, however, that this is not a simple aide-memoire; all successful education and learning involves structuring (even if this means rejecting it as the personality, events or knowledge evolve). But, as with everything, nothing is possible in the regulation of drugs and consumables without this initial structuring. This study has been presented in a didactic way to help with this. But of course, it doesn't come without work (a contrario, learning everything by heart is stupid, and learning a skeletal summary by heart is useless.

Autorentext

CIRIMWAMI Chancellor, PhD from Université Paris Nanterre and BIU/ Spain, Master in SSEnTS from Université de Versailles/France, Ph. at Université de Lubumbashi, /RDC, Ph.Inspecteur Provincial/Sud-Kivu, writer, Lecturer, EPN partner (Nairobi and Dar-es-Salaam),Former member of LAPPS (Paris) and lecturer at ISEAV, ISTM, UEA.