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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Negotiating Medical Device, Pharmaceutical, and Biotechnology Product Sales Contracts
Join Lisa Damhof, as she advises how a successfully negotiated contract hinges on understanding stakeholder priorities and finding common ground, with the ultimate goal of providing patients with access to the products they need.
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Changing Policies and Attitudes: Impacts on Medical Product Litigation
Join representatives from Holland & Knight LLP for a panel discussion on medical product litigation due to changing policies and attitudes.
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Claims 2025: Navigating an Increasingly Difficult and Complex World for Life Science Companies
Join Andy Hall and Ricky C. Benjamin, as they give an update on the claims and legal environment for life science companies.
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Ripped from the Headlines: Hot Topics in Life Sciences 2025
The life sciences industry is constantly changing, and equally dynamic are the challenges industry participants encounter. Join Medmarc's Risk Managers to discuss these changes from 2025.
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