Sarah is the Principal Consultant at LFH Regulatory. She holds a degree in Analytical Chemistry and began her career in the pharmaceutical industry, where she spent 12 years gaining extensive experience. She then transitioned into the medical device sector, working in regulatory roles for five years within various medical device companies.
For the past 10 years, Sarah has worked as a regulatory and quality consultant, supporting small to medium-sized medical device companies in achieving and maintaining regulatory compliance.
Her expertise spans the creation of technical documentation for Class I to Class III devices, including electromedical equipment, software as a medical device (SaMD), and life-supporting devices, for both EU and UK markets. She has also successfully supported numerous regulatory submissions and audits, including those related to ISO 13485 quality management systems.
She aims to continue providing expert, client-centric medical device support and advice to manufacturers wishing to place both established and novel devices on the market to meet existing and future patient needs.