Cabo Verde

Africa

Contents

1. Regulatory Overview
2. Regulatory Pathways

Regulatory Overview

Cabo Verde is regulated by the ARFA (Agência de Regulação e Supervisão dos Produtos Farmacêuticos). The country has 1 documented regulatory pathway for accessing unapproved or unlicensed medicines, covering named patient programs, compassionate use schemes, and special access arrangements.

Regulatory Authority

ARFA (Agência de Regulação e Supervisão dos Produtos Farmacêuticos)

Regulatory Pathways (1)

Cabo Verde MOH Special Import Authorization 45 days

Cabo Verde Ministry of Health special import authorization for unregistered medicines for patients with serious or life-threatening conditions.

Application Form: MOH Cabo Verde Special Import Form

Legal Basis: Regulated

Eligibility: Serious or life-threatening condition with no locally registered alternative

Cabo Verde

ISO Code	`CV`
Region	Africa
Regulatory Authority	ARFA (Agência de Regulação e Supervisão dos Produtos Farmacêuticos)
Pathways	1 documented
Drugs Available	0 documented