Regulatory pathway, options, and timing.
Learn about the differing regulatory pathways for devices, therapeutics, diagnostics, and digital health technologies. We’ll review the many variables in cost and timeline and what they mean to you and your technology. Come ready with questions for featured speaker, Richard diMonda.
Speaker, Richard diMonda, BEE, MSBME, MBA, brings over 30 years of medical device commercialization experience, from a variety of public and private medical companies, to new medical device and Health IT ventures. He has executive management as well as hands-on experience with regulatory, clinical research, reimbursement, product management and marketing.
This event is the sixth session in the Bench2Market talks series which was created to provide commercialization guidance to the university research community. Series topics include how to take your technology from the lab to commercial success and explore market opportunities surrounding entrepreneurial and innovative ideas.
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FAQs
Who Should Attend?
Events are open to entrepreneurs in the life sciences, GA CTSA, Georgia Tech and Emory University faculty, staff, graduate students, post-doc, residents and fellows.
Where can I find information about the entire Bench2Market Series?
For details and registration links for all events in the series, visit
How do I register for the Georgia CTSA Entrepreneurship Certificate?
Contact Gayathri Srinivasan at gayathris@emory.edu for additional information or to register.
Will the session be recorded?
Registered attendees will receive a link to view the recording after the session.