Human Factors in the Digital MedTech Era: The Usability of Connected Technology
Join EPAM as they explore how robust Human Factor practices can help teams navigate usability and compliance of products in an increasingly digital landscape.
Medical Device Submissions Series: Investigational Device Exemption (IDE) Workshop
Our in-depth device submissions workshops will provide real-world case studies, tips and best practices directly from FDA and industry experts.
Medical Device Submissions Series: Premarket Approval (PMA) Workshop
Learn key PMA Submissions strategies to build a strong submissions, align with FDA expectations, and reduce delays.
Medical Device Submissions Series: 510(k) & De Novo Workshop
Join industry leaders for the in-depth 510(k) & De Novo Workshop for real-world case studies, submissions tips and best practices.
QMSR Transition: Legal and Audit Perspectives
Join Hogan Lovells experts to learn how the FDA is set to reshape the medical device regulatory landscape with the introduction of the QMSR.
Attracting, Engaging, Hiring & Retaining Industry’s Top Talent
Join The Mullings Group to learn strategies for hiring top performers and how medtech teams attract and retain talent.
Why Now Matters: The Impact of Early Adoption of a Patient Access Program Solution
Join PRIA Healthcare to explore how a Patient Access Program can accelerate access and drive lasting medtech success.
Supreme Court Term in Review: Implications for the Medical Technology Industry
Supreme Court Term in Review: Implications for the Medical Technology Industry
Engineering the Future of MedTech with Insight-Driven Platforms
Discover how Medtronic, a global leader in medical technology, partnered with GlobalLogic and AWS to help engineer the Future of MedTech with Insight-Driven Platforms
Closing the Gender Health Gap: Driving Accountability through the [w]Health Index
Closing the Gender Health Gap: Join Kearney in discussion of how today’s women face a number of disadvantages in healthcare.