Global Medical Device Podcast powered by Greenlight Guru
Health & Fitness:Medicine
In this episode, Lisa Van Ryn, a seasoned expert from Greenlight Guru, shares her extensive knowledge on the FDA’s Medical Device Reporting (MDR). We unpack the nuances of when and how to report incidents, the definition of serious injuries, and the importance of effective complaint management systems. Lisa provides practical advice on setting up robust reporting processes and explains how manufacturers can avoid common pitfalls.
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Beginner’s Section: MedTech 101
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We value your thoughts! Please leave us a review on iTunes and share your feedback. Your suggestions help us improve and guide our future topics. Email your thoughts and topic suggestions to podcast@greenlight.guru.
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This episode is brought to you by Greenlight Guru, a leading platform that offers MedTech companies a comprehensive quality management software, designed to help navigate the complex landscape of medical device regulations.
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For more resources and information, visit the Global Medical Device Podcast...
#369: Advice to Medical Device Inventors
#368: Institutional Review Boards (IRBs)
#367: Interviewing the Interviewer
#366: Cardiac Arrest: Five Heart-Stopping Years as a CEO on the Feds Hit-List
#364: Building a Partnership with your Regulatory Consultant
#363: Bringing a Self-Funded Medical Device to Market
#362: Managing Risk in Clinical Investigations
#361: Speaking the Language of IVD
#360: Is It Possible to "Buy" a QMS?
#359: Project Management in MedTech
#358: FDAs Voluntary Improvement Program
#357: The State of UDI Across the World
#356: Quality Myths & Lessons Learned Part II
#355: Mastering the Pitch: MedTech Innovations from Concept to Market
#354: Advice for MedTech Regulatory Affairs Professionals
#353: How Artificial Intelligence is Impacting the MedTech Industry
#352: Fundamentals of Quality & Regulatory
#351: The State of AI & Clinical Investigations
#350: The Evolving Landscape of AI in MedTech
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