Assistant Chief Regulatory Officer, Drug Registration & Regulatory Affairs Directorate, Drug Registration Division, Variation

A highly motivated and experienced regulatory officer with over a decade of progressive experience in the pharmaceutical, food safety, and public health sectors. I am seeking to leverage my background in microbiology and my extensive training in regulatory affairs to contribute effectively to public health management and drug regulatory systems. I aim to enhance my current role at NAFDAC by applying my expertise in dossier review, compliance, and risk assessment to ensure public health is safeguarded through effective regulatory oversight.

As an Assistant Regulatory Officer at NAFDAC, I am passionate about ensuring that the drugs available in the market meet the highest standards of safety, efficacy, and quality. I have undergone multiple specialized trainings, including dossier review and Good Manufacturing Practices (GMP), which have enhanced my ability to assess drug product dossiers effectively. My continuous involvement in training programs and hands-on experience has strengthened my ability to lead teams in ensuring compliance with global regulatory standards. My goal is to continue contributing to public safety and regulatory excellence through leadership, knowledge dissemination, and professional growth.