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African Medical Devices Regulatory Harmonization Program

Food and Drug Administration

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Summary
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United States of America
Research, Development and Innovation
Overview

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.

Eligibility

Sole Source

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All information about this funding has been collected from and belongs to the funding organization
19 April 2023