Global Medical Device Podcast powered by Greenlight Guru
Health & Fitness:Medicine
In this episode of the Global Medical Device Podcast, host Etienne Nichols delves into the intricate world of in vitro diagnostics (IVDs) with Christie Hughes, a principal consultant and IVD expert at Qserve Group. With over 25 years of experience, Christie shares her extensive knowledge, discussing the nuances of IVDs, regulatory landscapes, and practical insights for professionals transitioning into or within the IVD sector.
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#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
#365: Medical Device Reporting: The Do's and Don'ts
#364: Building a Partnership with your Regulatory Consultant
#363: Bringing a Self-Funded Medical Device to Market
#362: Managing Risk in Clinical Investigations
#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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