Global Medical Device Podcast powered by Greenlight Guru
A podcast by Greenlight Guru + Medical Device Entrepreneurs - Lunedì
416 Episodio
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#334: MedTech Funding and Preparing for Due Diligence
Pubblicato: 31/08/2023 -
#333: Exploring Breakthrough Device Designation
Pubblicato: 25/08/2023 -
#332: Regulatory Strategy and the Advantage of Diversity in MedTech
Pubblicato: 17/08/2023 -
#331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues
Pubblicato: 10/08/2023 -
#330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?
Pubblicato: 03/08/2023 -
#329 The Right Way to Start a QMS: When, How, & What
Pubblicato: 27/07/2023 -
#328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices
Pubblicato: 20/07/2023 -
#327 Understanding the ROI of an eQMS
Pubblicato: 11/07/2023 -
#326 CSA vs. CSV: Modern Validation for Modern MedTech
Pubblicato: 07/07/2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Pubblicato: 30/06/2023 -
#325 The Role of dFMEAs in Risk Management for Medical Devices
Pubblicato: 29/06/2023 -
#324 Management Responsibility: The most important part of a QMS
Pubblicato: 22/06/2023 -
#323 The Combination Products Handbook
Pubblicato: 16/06/2023 -
Leaning into Lean Documentation
Pubblicato: 07/06/2023 -
Cybersecurity and the Future of MedTech
Pubblicato: 02/06/2023 -
How AI Can Help You Manage Risk
Pubblicato: 26/05/2023 -
Ad Promo and The Difference in Regulatory & Legal
Pubblicato: 24/05/2023 -
The Tools that Make Clinical Investigations
Pubblicato: 13/05/2023 -
Complaint Handling with Medical Device Guru, Brittney McIver
Pubblicato: 03/05/2023 -
Avoiding Potential Issues with your 510(k) Submission
Pubblicato: 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.
