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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Medical Device Design and Infection Prevention: What Do Manufacturers Need to Know?
A growing concern for healthcare providers is the expanding universe of drug-resistant microbes and the hospital-acquired infections that can result in complications, mortality, and morbidity....
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Medical Device Warnings for Home Use Devices
Given the current climate, home-use medical devices have become increasingly important, which is reflected in their unprecedented market growth this past year. Home-use medical devices offer users the...
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One Year Later: The PREP Act and COVID-19
In this special edition webinar series, Medmarc defense panel member, Jordan Lipp, Managing Member, Childs McCune, will lead an updated discussion about the PREP Act and COVID-19 a year later and...
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FDA Outlook: What to Expect in 2021
With the ongoing COVID-19 pandemic, a transition to the new Biden administration (including a new FDA Commissioner), and shifting control of the Senate, uncertainty remains the one constant. In this...
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