Global Medical Device Podcast powered by Greenlight Guru
Un pódcast de Greenlight Guru + Medical Device Entrepreneurs - Lunes
416 Episodo
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#334: MedTech Funding and Preparing for Due Diligence
Publicado: 31/8/2023 -
#333: Exploring Breakthrough Device Designation
Publicado: 25/8/2023 -
#332: Regulatory Strategy and the Advantage of Diversity in MedTech
Publicado: 17/8/2023 -
#331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues
Publicado: 10/8/2023 -
#330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?
Publicado: 3/8/2023 -
#329 The Right Way to Start a QMS: When, How, & What
Publicado: 27/7/2023 -
#328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices
Publicado: 20/7/2023 -
#327 Understanding the ROI of an eQMS
Publicado: 11/7/2023 -
#326 CSA vs. CSV: Modern Validation for Modern MedTech
Publicado: 7/7/2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Publicado: 30/6/2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Publicado: 29/6/2023 -
#324 Management Responsibility: The most important part of a QMS
Publicado: 22/6/2023 -
#323 The Combination Products Handbook
Publicado: 16/6/2023 -
Leaning into Lean Documentation
Publicado: 7/6/2023 -
Cybersecurity and the Future of MedTech
Publicado: 2/6/2023 -
How AI Can Help You Manage Risk
Publicado: 26/5/2023 -
Ad Promo and The Difference in Regulatory & Legal
Publicado: 24/5/2023 -
The Tools that Make Clinical Investigations
Publicado: 13/5/2023 -
Complaint Handling with Medical Device Guru, Brittney McIver
Publicado: 3/5/2023 -
Avoiding Potential Issues with your 510(k) Submission
Publicado: 27/4/2023
The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.
