Tony holds a master in Material Science Engineering and is certified in Clinical, Regulatory and Quality Affairs for Medical and In vitro Diagnostic devices. He worked as a regulatory affairs specialist in a neurotech startup company for over 5 years and gained significant experience in submission of complex technical documentation to both EU notified body and the FDA as well as an excellent understanding of the overall medical device life cycle.
In his free time, Tony enjoys practicing judo and is an active staff member in his club activities.
- Regulatory Affairs
- Risk Management
- Technical documentation
- Design Control
- Quality Management System
- Deep Brain Stimulation System
- Medical Device