Mahtab Fatemi joined Nuvaira in late 2012 with more than 14 years of experience in executing regulatory strategies for pharmaceuticals and medical devices. In her current role, she will develop and oversee corporate efforts to ensure that developed products meet the requirements of the US FDA and other international regulatory authorities.
Prior to joining Nuvaira, Ms. Fatemi ran an independent regulatory consulting business for four years where clients included Broncus Medical, a developer of diagnostic & therapeutic technologies to treat patients with lung disease. Ms. Fatemi spent two years at MAP Pharmaceuticals as Director of Regulatory Affairs overseeing both US and global submissions. She began her career as a Regulatory Affairs Specialist at BD Biosciences where she worked for seven years.
Ms. Fatemi holds a Bachelor of Science in Biology from the University of California, Irvine and a Master of Science degree in Physiology from Georgetown University. She also has a Juris Doctor from Santa Clara University and is currently a member of the California Bar.