At Insanity Labs, I support Quality Assurance and Regulatory Affairs activities for AI-based Software as a Medical Device (SaMD), including software verification, validation, and regulatory documentation.
At Adonmed Technology Solutions, I managed medical device regulatory submissions involving ISO 13485 and supported cosmetic and pharmaceutical product registrations.
I also assisted with hospital equipment planning and installation at Adonmed Technology Solutions.
Earlier, as a Biomedical Engineer Intern at Adonmed Technology Solutions, I trained in healthcare information software pre-sales, basic medical regulatory solutions support, and hospital biomedical technical solutions.
