Global Medical Device Podcast powered by Greenlight Guru
A podcast by Greenlight Guru + Medical Device Entrepreneurs - Lunedì
416 Episodio
-  #334: MedTech Funding and Preparing for Due DiligencePubblicato: 31/08/2023
-  #333: Exploring Breakthrough Device DesignationPubblicato: 25/08/2023
-  #332: Regulatory Strategy and the Advantage of Diversity in MedTechPubblicato: 17/08/2023
-  #331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain IssuesPubblicato: 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, & WhatPubblicato: 27/07/2023
-  #328 FDA Guidance on Artificial Intelligence (AI) in Medical DevicesPubblicato: 20/07/2023
-  #327 Understanding the ROI of an eQMSPubblicato: 11/07/2023
-  #326 CSA vs. CSV: Modern Validation for Modern MedTechPubblicato: 07/07/2023
-  #325 The Role of dFMEAs in Risk Management for Medical DevicesPubblicato: 30/06/2023
-  #325 The Role of dFMEAs in Risk Management for Medical DevicesPubblicato: 29/06/2023
-  #324 Management Responsibility: The most important part of a QMSPubblicato: 22/06/2023
-  #323 The Combination Products HandbookPubblicato: 16/06/2023
-  Leaning into Lean DocumentationPubblicato: 07/06/2023
-  Cybersecurity and the Future of MedTechPubblicato: 02/06/2023
-  How AI Can Help You Manage RiskPubblicato: 26/05/2023
-  Ad Promo and The Difference in Regulatory & LegalPubblicato: 24/05/2023
-  The Tools that Make Clinical InvestigationsPubblicato: 13/05/2023
-  Complaint Handling with Medical Device Guru, Brittney McIverPubblicato: 03/05/2023
-  Avoiding Potential Issues with your 510(k) SubmissionPubblicato: 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.
