Primary Job Title SVP of Regulatory Affairs Primary Organization 
SteadyMed Therapeutics
Location Montclair, New Jersey, United States Regions Greater New York Area, East Coast, Northeastern US Gender Male
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Mike has more than 25 years of research and development experience in the pharmaceutical and biotechnology industry.
Prior to joining SteadyMed, Mike held a variety of Regulatory Affairs, QA, Compliance and Project Management leadership positions at Upjohn, Pharmacia, Pfizer, CV Therapeutics, Ilypsa, Relypsa, and NextWave Pharmaceuticals.
He has successfully supported more than 30 US and worldwide IND and NDA applications across a broad range of therapeutic areas, including Quillivant XR (for ADHD), Kiklin (hyperphosphatemia), Ranexa (angina), Daxas (COPD/asthma), Depo-Provera SC (endometriosis/contraception), Xanax XR (anxiety), Genotropin (GH deficiency), Rescriptor (antiviral), and Colestid (hypercholesterolemia).
