I am Silas Amponsah Darko, a pharmacist and regulatory professional with expertise in the evaluation and regulation of biological and biotechnological products. At the Food and Drugs Authority (FDA), Ghana, I contribute to strengthening regulatory systems and advancing scientific oversight of biologics and biosimilars. As a Fellow of the GHPP PharmTrain2 Biosimilar Fellowship, in collaboration with BfArM, Germany, I actively engage in regional capacity-building initiatives aimed at enhancing biosimilar regulation across Africa. I am passionate about advancing regulatory science through training, mentorship, and collaboration, with a focus on improving access to quality biological medicines and contributing to sustainable global health outcomes.
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African Union Development Agency - AUDA-NEPAD
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