Upcoming Webinars
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Wearable and Home-use Devices Part 2: FDA Submissions
In this webinar, Tyler Ting, Director of Regulatory at Rook Quality Systems, walks you through the FDA submission landscape specific to wearable and home-use devices, so you can move from development to clearance with confidence.
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Past Webinars
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Best Practice to Navigate FDA Enforcement Actions
Are you prepared to respond if you are the subject of an FDA enforcement action? Do you know what types of FDA enforcement actions exist? If your business is manufacturing, repackaging, relabeling, and/or importing medical devices into the U.S. and you want to learn best practices to navigate potential FDA enforcement actions this webinar is for you.
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Life Sciences Claims 2023: Making sense of an evolving landscape
In this year’s annual year-end wrap-up, a panel including Andy Hall and Lauren Hulbert with Medmarc’s claims department, as well as Katie Stricklin, an attorney with Walsworth WFBM, LLP, will provide a claims and litigation year-end up wrap-up.
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Ripped from the Headlines: Hot Topics in Life Sciences
The life sciences industry is constantly changing, and equally dynamic are the challenges industry participants encounter.
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Importing Medical Devices into the U.S. in Compliance with the U.S. FDA
This webinar will provide a basic overview of FDA regulations and requirements to import medical devices into the U.S. Jennifer Diaz will discuss how the FDA defines and regulates a medical device and the pathway to legally market a medical device in the U.S.
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