Upcoming Webinars
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mRNA Patent Wars Update: Litigations Expand and Key Rulings Expected in 2025
Join Rothwell Figg Partner Dan Shores as he gives a mRNA patent wars update.
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Developing and Maintaining an FDA Compliant Complaint Handling Process
Join Sarah Lacey Robbins from RookQS as she discusses developing & maintaining an FDA compliant complaint handling process.
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Medical Device v2.0: Safer but Riskier?
Join Clark Hill PLC Member Matt Marshall as he discusses the requirements of GMP relating to product improvement, the potential risks of such improvements in litigation, and how such improvements may run afoul of a device’s existing FDA clearance.
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Past Webinars
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Introduction to Human Factors Engineering
Join Emergo by UL’s Human Factors Research & Design team to learn about the regulatory imperatives – and commercial benefits – associated with applying Human Factors Engineering (HFE) throughout medical device development.
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Sales Representative in the OR: Navigating a Liability Minefield for a 15-year Retrospective
15 years ago, Medmarc launched its very first Risk Management Webinar with presenter Eric Zalud on the topic of Sales Representatives in the OR: Navigating a Liability Minefield. For our 45th anniversary celebration we have invited back Eric to revisit this topic for a 15-year retrospective.
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Important Export Control Considerations for the Life Sciences Industry
Join us to learn about the nuts and bolts of export controls - including potential regulatory restrictions - confronting manufacturers and distributors of medical devices, pharmaceuticals, and other technologies who sell their products to foreign buyers.
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Mastering Your Next Audit: Proven Strategies for Success
Join Rook Quality Systems for an insightful webinar on mastering your next audit. Discover expert strategies and best practices to ensure compliance, streamline processes, and confidently navigate audits with success. Don't miss this opportunity to elevate your quality management approach and achieve excellence in regulatory assessments.
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