Felicia Hosey, RAC brings over two decades of hands-on experience in the medical device and in vitro diagnostics (IVD) sectors, helping companies navigate complex regulatory landscapes to achieve global market authorization and maintain compliance. Throughout her career, she has built a reputation for guiding clients from product concept to successful commercialization.
Felicia has supported the MedTech industry at every level — as an independent consultant, strategic contractor and regulatory leader within both startups and established organizations. Her expertise spans critical areas including global regulatory strategy, development of robust quality management systems, and execution of clinical studies. She holds a Regulatory Affairs Certification (RAC) and is an active member of the Regulatory Affairs Professionals Society (RAPS), credentials that underscore her commitment to professional excellence in a continually evolving regulatory environment.
Felicia’s deep understanding of the global regulatory landscape and her proven track record make her an invaluable asset to the Indie Medtech team. She is passionate about empowering innovators to bring life-changing technologies to market efficiently and effectively.
