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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Mitigating Product Liability Risk in the Era of COVID-19
The following topics will be covered in this webinar: Outlining potential product liability risk involving COVID (defect claims involving marketing/advertising, warranties, and warnings) Tips on...
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Force Majeure: COVID-19
This session we look at force-majeure clauses and how this frequently overlooked contractual language can be utilized should the pandemic interrupt your life sciences business operations.
Read More about As the country responds to the COVID-19 pandemic, life sciences companies as well as manufacturers that do not normally produce medical devices are coming together to fill the vast gaps in... -
Public Readiness and Emergency Preparedness Act (PREP Act)
As the country responds to the COVID-19 pandemic, life sciences companies as well as manufacturers that do not normally produce medical devices are coming together to fill the vast gaps in...
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Mitigating Cyber Risks in Digital Medical Devices: An Introduction
Digital medical devices employ some form of computing hardware and/or software. However, this technology can carry complex and very costly cyber risks that arise during product development and after...
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