Upcoming Webinars
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FDA QSR to QMSR: Regulatory, Legal, and Risk Implications for Industry
In this webinar, Denise Holliday, Expert Witness at Capwell Consulting Group, helps you understand how the transition to QMSR may affect regulatory compliance, product liability exposure, and organizational risk.
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Past Webinars
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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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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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