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Approve and register medicines and related products regulated under the Act, manufactured within or imported into, and intended for use in The Gambia.
Analyze the quality of medicines and related products to ensure that products meet quality standards. Currently can only outsource QC Testing.
Detect & report of product quality. Inspect premises to ensure that regulatory requirements and standards are enforced.
Monitor and report the safety of medicines and related products.
Examine, grant, issue, suspend, cancel and revoke import/export permits and license for Importers, Manufacturers, Storage Facilities and Repackaging.
Authorize and monitor clinical trials to ensure the protection of research participants and integrity of the data collected