I hold Masters degrees in both Biomedical Materials Science and Engineering and Advanced Neuroimaging. With over 15 years' experience in research, development and commercialisation of medical devices within a range of company types and sizes my expertise comprises a deep understanding of all aspects of the medical device lifecycle and associated regulatory requirements.

An ISO 13485 certified lead auditor, I combine targeted engineering knowledge with quality, regulatory and clinical affairs support tailored to your company and circumstances. Expert in active implantable medical devices, clinical trials and regulatory compliance, I am skilled in implementing pragmatic, efficient and scalable solutions that can accelerate your path to commercialisation.

Delivering clear and concise guidance based on technical, regulatory and commercial requirements mean that I deliver real value for clients.