Principal Regulatory Consultant
CardioMed Device Consultants
HERNDON, Virginia, United States
Mona Advani is a recognized Medical Device Consultant with 23 years of professional experience in domestic and international regulatory affairs with a focus on business strategic goals. She has consulted for a wide range of technology devices, previously holding titles of Senior Director of Regulatory Affairs and Clinical Research, Manager of Business Development, Manager of U.S. and International Regulatory Affairs. Mona has worked with small and large medical device companies, successfully focusing on the appropriate product development strategy for a wide variety of Cardiovascular, Neuro, Peripheral, AI/Software, and Structual Heart medical devices, both in the United States and internationally, including the European Union (EU), Japan and Canada.
Disclosure(s): No financial relationships to disclose
INNOVATIONS IN ARTIFICIAL INTELLIGENCE
Monday, March 10, 2025
8:00 AM – 9:00 AM ET
AI AND THE IMPACT ON CORONARY REVASCULARIZATION
Monday, March 10, 2025
9:00 AM – 9:40 AM ET
Welcome and Topic Introduction
Monday, March 10, 2025
9:00 AM – 9:02 AM ET
Panel Discussion | What is the Future of Software Medical Devices in Cardiology?
Monday, March 10, 2025
9:32 AM – 9:40 AM ET
Monday, March 10, 2025
9:40 AM – 10:37 AM ET
FUTURE TECHNOLOGIES UPDATE- SaMD
Monday, March 10, 2025
10:37 AM – 11:35 AM ET
Monday, March 10, 2025
11:19 AM – 11:35 AM ET
Monday, March 10, 2025
11:35 AM – 12:00 PM ET
Welcome and Topic Introduction
Monday, March 10, 2025
11:35 AM – 11:37 AM ET
Monday, March 10, 2025
12:09 PM – 12:25 PM ET
Panel Discussion | Digital Heath Apps in Clinical Trials: Ready for Prime Time?
Tuesday, March 11, 2025
11:30 AM – 12:00 PM ET