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Completing the set of interactive submissions workshops, industry and FDA experts will lead you through the strategic considerations and practical steps of filing a Premarket Approval.
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During this interactive workshop, FDA and industry experts will lead you through the regulatory and practical guidelines governing when an investigational device exemption (IDE) is required.
... moreFDA and industry experts are coming together to review the basics of 510(k) submissions. This unique opportunity will help you better understand the FDA perspective on 510(k) submissions, from proc... more
Led by industry and FDA experts, this workshop will provide an in-depth overview of how organizations can best tackle complaints, MDRs and recalls. Together with industry and FDA experts, we've dev... more
November 7, in Arlington, Virginia, AdvaMed will host our inaugural, AdvaMed Health Data Stewardship & Privacy Summit, bringing together leading experts and health care industry stakeholders to... more
On November 6, in Arlington, Virginia, AdvaMed will host our annual Cybersecurity Summit, bringing together experts across the device security spectrum. Speakers will provide in-depth and timely up... more
On October 24, from 12-1p ET, AdvaMedDx will co-sponsor a Capitol Hill briefing focused on how stakeholders can best partner to address the antimicrobial resistance (AMR) threat. Other co-sponsors... more
The MedTech Conference will bring together more than 3,000 attendees to network, conduct business, gain access to capital, and share insights in Boston, MA, from Sept. 23–25.
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The Next Generation Dx Summit is a nexus for key decision-makers, bringing together industry leaders with academic and clinical researchers to learn the latest technologies, assays, detection metho... more
Please plan to join AdvaMedDx this summer in Anaheim, CA, for our annual Diagnostic Leaders Unplugged Panel Session held in conjunction with the AACC Annual Meeting and Clinical Lab Expo. We look f... more