Associate Director, Global Regulatory Affairs
Johnson & Johnson, Vlaams-Brabant, Belgium
Marina holds a PhD in Biology and has built a successful career path in Quality and Regulatory Affairs for Medical Devices and In Vitro Diagnostics (IVDs) since 2007. Over the years, she has held various roles across multiple companies, progressively broadening her expertise in the field.
Currently, at Johnson & Johnson, Marina serves as a Global Regulatory Affairs Associate Director, specializing in clinical trial assays used in medicinal clinical trials, combined trials and assays developed as Companion Diagnostics for Precision Medicines. In addition to her role at Johnson & Johnson, Marina is an active member of the MedTech Europe trade association and serves on the leadership team of the Belgian RAPS Local Networking Group.
Tuesday, May 5, 2026
08:30 - 16:00 WEST
COMBINE: Navigating the Latest Trends in Combined Trials
Thursday, May 7, 2026
10:45 - 11:45 WEST
Mastering EU in-house tests: Real-World Lessons From Laboratories Under the IVDR Article 5(5)
Friday, May 8, 2026
12:30 - 13:30 WEST