Josephine is a Medical Writer at LFH Regulatory. After gaining a BSc Biomedical science degree she has gone on to work in various roles within pharmacovigilance, public health surveillance and regulatory affairs. She began her career in 2021 as a medical writer at a Biotechnology company, where she gained experience in writing technical documentation including STED files and Performance Evaluation documentation for a portfolio of clinical microbiology devices. She has developed her knowledge of IVD regulations and requirements.
She has since developed an interest in the medical device industry and its value to the advancement of patient healthcare. She is continuing to expand her technical writing skills and IVD knowledge by managing, writing and reviewing Performance Evaluation documentation for multiple projects across a portfolio of varying IVDs, as well as providing valuable expertise.
