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Co-Editor-in-Chief/Managing Partner for @MedTechStrat & @Market_Pathways. We offer #medtech executives with actionable intelligence & unparalleled perspective.
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ALT Medtech has been accelerating innovation in product development with a record 124 new #devices approved by the FDA in 2023. Yet, this speed is not matched in #medtech trials, which can take up to seven years to complete. By Nicole Bongers, @veevasystems: https://bit.ly/3FnXkJU
ALT Federal agencies including #FDA have retreated from various forms of public and stakeholder engagement during the opening weeks of the Trump administration. In #medtech, that’s starting to impact global standards development efforts and more: https://bit.ly/3F4L0OL
ALT NEW EP. of @Market_Pathways Podcast: Following a robust 2024, the medical device sector continues to thrive in 2025 and remains somewhat insulated from dramatic shifts in #healthcare policies, at least in the short term: https://bit.ly/42nb0hG
ALT Be the expert in the room. Stay ahead of the curve in #medtech regulatory, reimbursement, and policy with Pathways' Document Depot: https://bit.ly/4kCLqMi
ALT Ortho, spine, and #medtech are thriving, but elective procedures face economic and political uncertainties. @MedTechStrat talks with @ThisIsBTIG's Ryan Zimmerman on the 2025 outlook and what he hopes to learn at AAOS 2025 (March 10-14, San Diego): https://bit.ly/3FcPUt1
ALT #Robotics pioneer @IntuitiveSurg continues to be the dominant player with greater than 80% market share, nearly 10,000 da Vinci systems placed, and revenue growth in the mid to high teens, more than 20 years after it introduced the da Vinci robot: https://bit.ly/4hg6bum
ALT Explore the barriers and opportunities learn directly from key decision-makers and read stories of companies that are persevering along every pathways of the #medtech market with @Market_Pathways. Learn why you need us for your market access strategy: https://bit.ly/46Q3lIz
ALT $45M investment. 7,000+ life sciences jobs. Rhode Island is building a #MedTech hub, led by Mark A. Turco, M.D. What lessons has he learned, and what’s next for RI’s #lifesciences future? Learn more here: https://bit.ly/4jQIdsf
ALT Europe just enacted new requirements for device manufacturers to report anticipated product supply disruptions, and @US_FDA wants the US Congress to follow suit: https://bit.ly/4jygqwn #MedTech
ALT Will the U.S. follow Europe’s lead on device shortage reporting This compares the EU’s new Article 10a, which mandates proactive reporting, to the U.S.’s PHE-tied approach. Without broader mandates, the U.S. risks falling behind: https://bit.ly/4jygqwn #regulatory