Webinar: FDA regulatory strategy and value proposition for better medical product development
Join TSG's Laurie Clarke, along with Rob Morgan and Eduardo von Ristow from our sister company Sagentia Innovation, for this panel discussion focusing on real issues faced by those involved in developing, assuring compliance and quality, investing in, and marketing medical devices. The team will answer questions on how to navigate the 510(k), de novo, and PMA routes to market, translating concepts into products and maximizing success by better understanding different stakeholders' needs, technology feasibility and commercial viability.
Want to submit a question to our panel in advance? Email us at email@example.com