Regulatory affairs expert
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I have over 13 years of working experience as a regulatory expert in some NMRAs in Africa. My skills range from dossier compilation to scientific assessment of applications for registration of medicines as well as GxP inspections. Passionate about contributing to pharmaceutical development, regulation and marketing to ensure sustainable human and animal health.
13 years working experience ranging from dossier assessment to GxP audits among other roles
Postgraduate in medicines development, Masters in vaccinology and pharmaceutical clinical development, strategy management and management development program.
