Global Medical Device Podcast powered by Greenlight Guru
A podcast by Greenlight Guru + Medical Device Entrepreneurs - Luni
416 Episoade
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#334: MedTech Funding and Preparing for Due Diligence
Publicat: 31.08.2023 -
#333: Exploring Breakthrough Device Designation
Publicat: 25.08.2023 -
#332: Regulatory Strategy and the Advantage of Diversity in MedTech
Publicat: 17.08.2023 -
#331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues
Publicat: 10.08.2023 -
#330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?
Publicat: 03.08.2023 -
#329 The Right Way to Start a QMS: When, How, & What
Publicat: 27.07.2023 -
#328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices
Publicat: 20.07.2023 -
#327 Understanding the ROI of an eQMS
Publicat: 11.07.2023 -
#326 CSA vs. CSV: Modern Validation for Modern MedTech
Publicat: 07.07.2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Publicat: 30.06.2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Publicat: 29.06.2023 -
#324 Management Responsibility: The most important part of a QMS
Publicat: 22.06.2023 -
#323 The Combination Products Handbook
Publicat: 16.06.2023 -
Leaning into Lean Documentation
Publicat: 07.06.2023 -
Cybersecurity and the Future of MedTech
Publicat: 02.06.2023 -
How AI Can Help You Manage Risk
Publicat: 26.05.2023 -
Ad Promo and The Difference in Regulatory & Legal
Publicat: 24.05.2023 -
The Tools that Make Clinical Investigations
Publicat: 13.05.2023 -
Complaint Handling with Medical Device Guru, Brittney McIver
Publicat: 03.05.2023 -
Avoiding Potential Issues with your 510(k) Submission
Publicat: 27.04.2023
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.
