Goodwin on Medtech

Insights and resources covering the latest medtech trends influencing your business

Goodwin’s global Medtech practice is a one-stop shop for innovators bringing breakthrough medical technologies to market, providing comprehensive guidance on everything from corporate and transactions to intellectual property strategy and regulatory compliance. Explore our latest perspectives.

Regulations
Antitrust and Competition Life Sciences Year in Review 2025
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Intellectual Property
What European Medtechs Should Know About the US Patent System
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Regulations
US Emerging as Top Global Medtech Destination
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Corporate and Transactional
Fundraising Strategies for Early-Stage Medtech Startups
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Corporate and Transactional
Medtech M&A and VC Signal Positive Momentum Entering 2025
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Intellectual Property
Four Steps to Maximize the Value of AI Innovation in Medtech
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Regulations
How the EU AI Act Could Affect Medtech Innovation
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Regulations
Quarterly Issue Tracker: Life Sciences Regulations — Q1 2025 and Beyond
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Regulations
FDA Approvals of AI Medical Devices Rise Rapidly
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Intellectual Property
Inventing With AI
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Regulations
The FDA’s 510(k) Program Guidance: Predicate Device Selection and Clinical Data Usage
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Regulations
Avoid FDA Misbranding: Correct Terms for 510(k) Devices
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Past Medtech Events