Kirsty Louise Marrow

Kirsty Louise Marrow is an experienced regulatory and quality assurance professional with a robust background in the medical devices and biotechnology sectors. Currently serving as a Regulatory Affairs Clinical Data Manager at Biocomposites, Kirsty has previously held significant roles including Global Regulatory Affairs Manager at H&T Presspart and QSHE & Regulatory Manager at Prestige Medical Ltd, where oversight of quality assurance for class II medical devices was a key responsibility. Other roles include UK Quality Assurance Manager at Neogen Corporation and Clinical Trials Manager at the Clinical Trials Research Centre. Kirsty possesses a Master's degree in Quality Systems Management from the British Standards Institute and a Dip HE in Equine Veterinary Science from Harper Adams University, alongside qualifications in Geology/Earth Science and Science.