Cherry Malonzo Marty is a Medical Doctor and Biomedical Engineer by training. She has more than 12 years of experience working in various functions in education, clinical settings, research, and regulatory affairs.

Since 2018, she has been working as a contract regulatory writer and consultant for medical device, combination product, in vitro diagnostics (IVD), and Software as a Medical Device (SaMD) submissions in the US and EU, handling Class I to Class III devices across a range of medical applications. Since 2021, Cherry is the module leader for International Regulatory Affairs at the Sitem Center for Translational Medicine and Biomedical Entrepreneurship in Bern, Switzerland. She has co-authored the book chapter “Evolving Global Regulatory Landscape” in the 1st edition of The Combination Products Handbook published in 2023.

Cherry co-leads the EMWA workshop Introduction to Combination Products in the US and the EU.