Svetlana Mukhina

Merck

Dr. Svetlana Mukhina is Manager Global Regulatory Affairs, Biomarkers and Diagnostics at Merck KGaA, where she is leading global CDx regulatory activities for two development programs. In this role, she closely works with companion diagnostic development manufacturers and internal stakeholders to develop regulatory strategies enabling IVD / therapeutic codevelopment. Svetlana holds a PhD in Biology and an MSc in Regulatory Affairs, with a focus on regulation of in vitro companion diagnostic devices in the US. Overall, she has 16+ year experience in molecular oncology, drug discovery, and assay development.
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