Fiona Gould

IVDR Quality And Regulatory Affairs Consultant at Debiopharm

Fiona Gould is an experienced professional in Regulatory Affairs and Quality Management Systems, currently serving as a Quality Assurance Consultant at Creonate Manufacturing since January 2023 and a Regulatory Affairs Consultant at Oxford Cancer Analytics since April 2022. Fiona has held various consultancy roles, providing expertise in IVD development and regulatory compliance, including the management of IVDR and MDR transitions for several organizations such as AnteoTech and Omega Diagnostics Group. With a strong foundation in science, Fiona holds a PhD in Cell and Molecular Biology from the University of Aberdeen, an MSc in Genetics from the University of Glasgow, and a BSc(Hons) in Applied Biological Sciences from the University of the West of England.

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