SRUTHI SUNDARAM
Regulatory Affairs Specialist
Sruthi Sundaram is a Regulatory Affairs Specialist at MDC Associates. Sruthi is a Ph.D. Pharmacologist with four years of regulatory and clinical strategy experience for investigational new drugs (IDN) or device exemptions (IDE). She received her doctoral and master’s degree from St. John’s University. Before joining MDC, Sruthi was a Senior Regulatory Scientist at Velico Medical, Inc., where she was responsible for supporting IND/IDE submissions and approvals to introduce new transfusion products to domestic and international markets.
