After a decade of doing research in nanomedicine and nanomaterials across Europe, in 2018 I stopped looking through microscopes, but continued to focus on the details that reveal the big picture.
I now help manufacturers navigate the labyrinth of the Medical Device Regulation (MDR) requirements.
I have covered a wide variety of clinical areas, including but not limited to urology, cardiology, wound management, neurosurgery, gastroenterology, emergency medicine and orthopaedics. I am always looking to expand my area of expertise.
I learned the ins and outs of the regulatory labyrinth servicing established manufacturers in the medical device industry at the time when we were all finding our way from MDD to MDR. Almost a decade later, I still relish the challenge of a complex device portfolio.
In more recent years, I found excitement in the startup environment, where I get to work closely with the people behind smart ideas to improve the lives of patients. First-hand access to those stories that prompt positive change is always an inspiration.
