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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Life Sciences Claims 2022: Redefining Normalcy
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 Jennifer Heis, an attorney with Ulmer Berne, will provide a claims...
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EUAs, 510(k)s and De Novos Demystified: Bringing COVID-19 Tests to the US Market
COVID-19 test developers and regulatory bodies rose to the challenge of quickly supplying the public with the tests necessary to determine infection status. However, many of these tests were brought...
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Increasing Diversity in Clinical Trials: FDA Guidance and Industry Efforts
This webinar will discuss efforts to increase enrollment in clinical trials of people from underrepresented racial and ethnic populations. We will discuss the latest FDA actions as well as efforts...
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Hot Topics in Life Sciences: What does this mean for products liability?
In this installment of Medmarc’s webinar series, Kate Klaus and Zuhal Reed, our attorneys from Medmarc’s Risk Management Department will guide a discussion on some of the top life sciences news...
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