Tanima Ghosh is the Director of Regulatory Affairs and Quality at Prenuvo, where she applies her extensive global experience in highly regulated industries, including Medical Devices, Pharmaceuticals, Undersea Telecommunications, and Space & Defense. Her expertise spans quality assurance, ideation, clinical IDE, new product introduction (NPI), research, design & development, operations, and regulatory affairs, with a focus on AI/ML and Software as a Medical Device (SaMD).