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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Managing Risks through IP Innovation Management Training
A recent survey of 1,500 global innovation executives revealed that innovation management continues to be a top priority. IP Innovation Management Standard 56005 is a global framework that can help companies consistently identify, manage, and mitigate their on-going risks and opportunities related to intellectual property.
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The mRNA/Lipid Nanoparticle Competitive and Litigation Landscape
While the COVID-19 pandemic caused tragedy for millions of families worldwide, it has also spurred concomitant advancements in health care, not the least of which include the first-ever regulatory approvals of therapies based on messenger RNA (mRNA) technology granted to Moderna and BioNTech (in collaboration with Pfizer).
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Artificial Intelligence Litigation Risks for the Medical Technology Industry
While the world is abuzz about artificial intelligence and the advances it will provide in the medical technology space, it is important to realize that along with the advances come risks—including litigation risks. There are numerous legal claims that have already started to piggyback on the growing adoption of artificial intelligence.
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From Hospital to Home: Mastering Home-use Medical Device Warnings and Labels
By exploring critical aspects of product liability and risk mitigation strategies, this presentation aims to educate companies on home-use medical device labels and warnings to protect interests while ensuring consumer safety.
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