Aug 26, 2021
You’ve got a great idea for a
medical device! Now what?
Most errors in clinical trials are a
result of poor planning. Fancy statistical methods cannot rescue
design flaws. Thus careful planning with clear foresight is
absolutely crucial for clinical trial success. With the
explosion of Medtech opportunities for startups, what are the
current best standards for ensuring the success of your design and
clinical trials?
Join us for this Live-Recorded
Podcast Event "Proving Your Device Works in The Real World" as we
discuss...
- Consideration for the problem
you are trying to solve
- Big Questions to answer for
Clinical Literature, IP Landscape, Stakeholder and Value
Proposition, What is relevant today
- Pre-clinical / Clinical Testing
Feasibility
- Planning the Clinical Trial Design
– Tactical and Strategic Considerations
- Regulatory Pathway & Business
Strategy
- Design Approach and policy level
considerations
- The External
Environment (Legislative, Healthcare Economics, Orange County
Talent, Reimbursement and Market Adoption
Expert Panelists
Include:
Dr. Michael Drues -
President of Vascular Sciences & FDA Consultant
Jeremy Koehler - Director Of
Engineering at NXT Biomedical
Vinny Podichetty - VP Clinical &
Medical Affairs at JenaValve Technology, Inc.
Anand S. Patel, MD - Chief of
Interventional Radiology at Providence Little Company of Mary,
Torrance
Free Opinion Disclaimer
The views and opinions expressed at this event are those of the
panelists and do not necessarily reflect the official policy or
position of their respective organizations. Any content
provided by our panelists are of their opinion and are not intended
to malign any organization, company, individual or any
entity.