Cherry Malonzo Marty is an MD and Biomedical Engineer by training. She has over 10 years of experience working in various functions in education, clinical settings, research, and regulatory affairs. She has co-authored the book chapter “Combination Products Evolving Global Regulatory Environment” in the 1st edition of The Combination Products Handbook published in 2023. Since 2019, she has been working as a freelance regulatory writer and consultant for medical device and combination product submissions in the US and EU. Since 2021, she is the module leader for International Regulatory Affairs at the sitem Center for Translational Medicine and Biomedical Entrepreneurship in Bern, Switzerland. Apart from her freelancing projects, she currently works part-time as the Regulatory and Quality writer for a spin-off of ETH, Zürich.