Ekaterina Riabova
Quality and Regulatory Consultant

Ekaterina has 8 years of experience in medical device/IVD new product development and product improvement projects. Specific competence in design documentation and V&V activities. She quickly grasps new issues and has worked several years with technical file documentation, regulatory support, vigilance reporting and global registrations.

Ekaterina has a researcher background and holds a Ph.D. in Bioinorganic Chemistry and a M.Sc. in Enzymology.