Global Medical Device Podcast powered by Greenlight Guru

368 Episoder

1. #346: FDAs eSTAR Program

   Publisert: 30.11.2023
2. #345: Using AI In MedTech

   Publisert: 22.11.2023
3. #344: Becoming an Advisor to a Medical Device Company

   Publisert: 16.11.2023
4. #343: Recent FDA Draft Guidances

   Publisert: 9.11.2023
5. #342: Planning an FDA Submission

   Publisert: 2.11.2023
6. #341: What NOT to say to FDA

   Publisert: 25.10.2023
7. #340: LDTs & the FDAs Proposed Ruling

   Publisert: 19.10.2023
8. #339: UDI and the State of EUDAMED

   Publisert: 12.10.2023
9. #338: Site Selection for Clinical Trials

   Publisert: 6.10.2023
10. #337: Moving MedTech Forward - The Past, Present & Future of Greenlight Guru

    Publisert: 21.9.2023
11. #336: From Academia to FDA Clearance (True Quality Roadshow - Boston)

    Publisert: 14.9.2023
12. #335: Accelerating SaMD Development in a Compliant Agile way

    Publisert: 8.9.2023
13. #334: MedTech Funding and Preparing for Due Diligence

    Publisert: 31.8.2023
14. #333: Exploring Breakthrough Device Designation

    Publisert: 25.8.2023
15. #332: Regulatory Strategy and the Advantage of Diversity in MedTech

    Publisert: 17.8.2023
16. #331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues

    Publisert: 10.8.2023
17. #330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?

    Publisert: 3.8.2023
18. #329 The Right Way to Start a QMS: When, How, & What

    Publisert: 27.7.2023
19. #328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices

    Publisert: 20.7.2023
20. #327 Understanding the ROI of an eQMS

    Publisert: 11.7.2023