Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

1. Pros & Cons of Being a Physician turned MedTech Inventor

   Gepubliceerd: 13-4-2021
2. 3 Systems of Risk for Medical Devices from FDA

   Gepubliceerd: 7-4-2021
3. Quality Management for IVD Devices vs Medical Devices

   Gepubliceerd: 5-4-2021
4. Understanding the Investigational Device Exemption (IDE) Process

   Gepubliceerd: 31-3-2021
5. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

   Gepubliceerd: 30-3-2021
6. Why the PMA Process is so Dreaded by Manufacturers in the US Market

   Gepubliceerd: 25-3-2021
7. Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

   Gepubliceerd: 24-3-2021
8. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

   Gepubliceerd: 21-3-2021
9. Meet a Guru: Sara Adams

   Gepubliceerd: 17-3-2021
10. Building a Startup in the MedTech Industry

    Gepubliceerd: 10-3-2021
11. Meet a Guru: Karen Schuyler

    Gepubliceerd: 8-3-2021
12. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Gepubliceerd: 4-3-2021
13. Everything you Need to Know about SaMD from an FDA Perspective

    Gepubliceerd: 1-3-2021
14. Preparing for Remote and On-Site Inspections and Audits

    Gepubliceerd: 24-2-2021
15. How does EU MDR impact your Quality Management System?

    Gepubliceerd: 22-2-2021
16. Virtual Auditing in a Post-COVID World of Digital Compliance

    Gepubliceerd: 18-2-2021
17. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Gepubliceerd: 10-2-2021
18. Prioritizing Medical Device Reimbursement During Product Development

    Gepubliceerd: 4-2-2021
19. 5 Actionable Lessons Learned from the RADx Initiative by NIH

    Gepubliceerd: 27-1-2021
20. What are the Strategic Priorities for CDRH in 2021?

    Gepubliceerd: 20-1-2021