Time: 1:30 PM to 3:30 PM
Description
A significant barrier to the successful commercialization of medical devices lies in the limited understanding of market valuation, supply chain management, and Medicare reimbursement. Biomaterials scientists should play a more prominent role, alongside clinicians, in shaping regulatory policies to ensure fair and accurate valuation. Without their expertise, there is a substantial risk of device mispricing, which can limit both their clinical impact and the broader influence of the biomaterials field.
To strengthen our professional community and elevate the
standing of our organization, it is essential for
scientists to actively engage in the commercial and
regulatory landscape.
This objective will be addressed through an open panel
discussion aimed at identifying and analyzing key
challenges faced by developers of biomaterial-based
medical devices. A particular focus will be on the
difficulty of conveying advanced scientific information to
payers such as the CMS, which currently rely predominantly
on clinical input, with minimal involvement from
biomaterials scientists.
Moderators:
Dr. Subramanian Gunasekaran
BMPC SIG, SFB
President, Encoll Corp
Murugan Gunasekaran
VP Sales & Marketing
Encoll Corp
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Talk by Joe Rolley, JTR Business Consulting, LLC Open Talk by Joe Rolley, JTR Business Consulting, LLC configuration optionsEditDelete Speakers Joe Rolley
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Talk by Murugan Gunasekaran, Encoll Corp. Open Talk by Murugan Gunasekaran, Encoll Corp. configuration optionsEditDelete Speakers Murugan Gunasekaran
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Talk by Subramanian Gunasekaran, Encoll Corp. Open Talk by Subramanian Gunasekaran, Encoll Corp. configuration optionsEditDelete Speakers Dr. Subramanian Gunasekaran
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Talk by Traci Kimball, The Wish Clinic Open Talk by Traci Kimball, The Wish Clinic configuration optionsEditDelete Speakers Dr. Traci Kimball