Woman-founded and led, Femasys combines internally developed innovation with in-house manufacturing expertise to ensure the quality, scalability, and successful commercialization of transformative women’s health solutions globally.
Vice President, Regulatory Affairs
Ms. Indeglia brings over 15 years of medical device industry experience in regulatory affairs and global clinical trial execution, securing regulatory approvals and enabling product launches. She has expertise in regulatory strategy, post-market surveillance, and clinical development across Class II/III devices and combination products. Prior to joining Femasys, she served as Global Vice President of Regulatory Affairs at Terumo Aortic, formerly Bolton Medical. Earlier in her career, she held roles of increasing responsibility at Atrium Medical, Wright Medical Technology, and RTI Biologics. Ms. Indeglia holds RAC certification from the Regulatory Affairs Professionals Society and is a Certified Tissue Bank Specialist through the American Association of Tissue Banks. She earned a BS in Chemical and Biomolecular Engineering from Johns Hopkins University and MS degrees in Chemical Engineering and Biomedical Engineering from the University of Florida.
