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
WHAT IS THE FUTURE LANDSCAPE? UNDERSTANDING AI AND SOFTWARE DEVICES IN CARDIOLOGY
Monday, March 11, 2024
9:00 AM – 9:47 AM ET
Monday, March 11, 2024
9:00 AM – 9:02 AM ET
Panel Discussion: What is the future of Software Medical Devices in the Cath Lab?
Monday, March 11, 2024
9:26 AM – 9:45 AM ET
Monday, March 11, 2024
9:45 AM – 10:45 AM ET
Monday, March 11, 2024
10:19 AM – 10:45 AM ET
WHAT ARE THE PRODUCT DEVELOPMENT AND REGULATORY CHALLENGES IN GETTING A SAMD TO MARKET?
Monday, March 11, 2024
10:45 AM – 11:20 AM ET
Monday, March 11, 2024
11:03 AM – 11:20 AM ET
DIGITAL PARTNERSHIPS AND MARKETING INVESTMENTS – WHAT WILL IT TAKE TO ADOPT SOFTWARE DEVICES?
Monday, March 11, 2024
11:20 AM – 12:00 PM ET
Monday, March 11, 2024
11:20 AM – 11:22 AM ET
Monday, March 11, 2024
11:46 AM – 12:00 PM ET
Summary from the Digital Health CRT 2024 Session
Tuesday, March 12, 2024
10:38 AM – 10:46 AM ET
Panel Discussion: Digital Heath Apps in Clinical Trials: Ready for Prime Time?
Tuesday, March 12, 2024
10:54 AM – 11:32 AM ET