African Medical Devices Regulatory Harmonization Program
The purpose of this program is to enable harmonized approaches, standards and guidelines in order to strengthen innovation, development, regulation and availability of medical devices that meet quality and safety requirements in the African continent. These efforts are critical to ensure consistent and aligned practices for the regulatory oversight of medical devices and to prevent the use or export of poor quality products that can lead to health consequences and increased expenditures.
Change history
First seen 28 Sept 2026, last checked 28 Sept 2026. 1 recorded version.
- 28 Sept 2026 · 2434d4efcd55