Trained as a physician with a background in trauma and orthopedic surgery, Katharina Friedrich moved from clinical practice into regulatory medical writing, focusing on MDR-compliant documentation for medical devices. In 2021, she founded her own consultancy to support medical device manufacturers with clinical evaluations and PMCF strategies. Since then, she has delivered over 100 clinical evaluation projects for more than 30 companies worldwide, working with clients from start-ups to established enterprise manufacturers. She also regularly contributes as a speaker and workshop leader at conferences and online events in Life Sciences.