What is FDA equivalent in Africa?

In the realm of healthcare and regulatory frameworks, the Food and Drug Administration (FDA) in the United States serves as a vital gateway for approving drugs, medical devices, and other health-related products for safety and efficacy. However, when we turn our gaze to the vast continent of Africa, the question arises: What is the FDA's equivalent? Does Africa have a unified regulatory body akin to the FDA, or does each country maintain its own set of standards and approval processes? With a diverse array of countries and cultures, it's imperative to understand how medical products are evaluated and regulated in this region. Could you elaborate on the regulatory landscape in Africa and provide insights into its potential FDA counterparts?