Megha Dali

Megha Dali currently serves as a Regulatory Affairs Specialist at Mizuho OSI since February 2025, following a brief tenure as a Regulatory Affairs and Quality Assurance Associate at Straumann Group, where a comprehensive gap analysis of standard operating procedures against regulatory frameworks was conducted. Prior experience includes a Regulatory Affairs Co-Op at Nova Biomedical, where leadership was demonstrated in managing Canadian Class II and III Medical Device License Amendments, and an experiential project as a Clinical Affairs Associate at Gel4Med, Inc., focusing on 510k approved Class II Medical Devices. Megha's foundational experience in safety operations spans roles at IQVIA, encompassing study team leadership and adverse event reporting. Megha holds a Master’s degree in Regulatory Affairs from Northeastern University and a Bachelor of Pharmacy from PES College of Pharmacy.