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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Ripped From the Headlines: A(n Eventful) Year in Review
In this installment of Medmarc’s webinar series, Kate Klaus, an attorney and FDA specialist in our Risk Management department, will guide a discussion of the top life sciences news stories of the...
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The Potential Life Sciences Implications of the Election
The medtech industry has significantly changed during the Trump administration’s last four years. FDA processes are streamlined, the medical device excise tax repealed, and the Senate is in the...
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How to Write Effective and Compliant Standard Operating Procedures (SOPs)
In this session, presenter, Joy McElroy from McElroy Training and Consultancy, will discuss the benefits of good technical writing, how to write effective and compliant SOPs using the correct...
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Clinical Trials in The Era of COVID-19
This session presenters, Dianne Bourque and Benjamin Zegarelli from Mintz, will explore the widespread disruptions the crisis is posing to clinical trials for life sciences companies and to research...
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