Michelle Coffey

Michelle Coffey, has over 20 years global experience in the pharmaceutical industry (Chemical and Biological), covering the life cycle of a product from early stage clinical right through to commercial launch and maintenance. She has extensive knowledge in global regulatory requirements, working on areas including emerging treatments and clinical protocols for cell therapy products and technologies. She has worked on cross-functional teams in order to develop effective product strategy, and ensure submission timelines and global regulatory requirements are met.