Oxana Razina is an accomplished Regulatory Affairs Professional with extensive experience in the pharmaceutical and healthcare industries. Oxana specializes in authoring, maintaining, and managing global product information and ensuring compliance with international regulatory standards.
With a proven track record at leading organizations such as GlaxoSmithKline, Takeda, Reckitt Benckiser, and Roche, she has demonstrated expertise in regulatory labelling, compliance, and strategic regulatory affairs. Oxana has played a key role in managing the lifecycle of global product information, preparing regulatory submissions, and ensuring alignment with national and international guidelines.
Her deep understanding of pharmaceutical regulations is complemented by her ability to collaborate across global teams, streamline processes, and deliver high-quality results.
Oxana holds a Master's degree in Pharmacy from Moscow Medical Academy and an MSc in Biotechnology from the Academy of Pure Chemical Technologies. Her educational background, coupled with her regulatory expertise, positions her as a valuable asset in the highly regulated pharmaceutical sector.
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