Global Medical Device Podcast powered by Greenlight Guru

416 Odcinki

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

   Opublikowany: 13.04.2021
2. 3 Systems of Risk for Medical Devices from FDA

   Opublikowany: 7.04.2021
3. Quality Management for IVD Devices vs Medical Devices

   Opublikowany: 5.04.2021
4. Understanding the Investigational Device Exemption (IDE) Process

   Opublikowany: 31.03.2021
5. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

   Opublikowany: 30.03.2021
6. Why the PMA Process is so Dreaded by Manufacturers in the US Market

   Opublikowany: 25.03.2021
7. Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

   Opublikowany: 24.03.2021
8. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

   Opublikowany: 21.03.2021
9. Meet a Guru: Sara Adams

   Opublikowany: 17.03.2021
10. Building a Startup in the MedTech Industry

    Opublikowany: 10.03.2021
11. Meet a Guru: Karen Schuyler

    Opublikowany: 8.03.2021
12. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Opublikowany: 4.03.2021
13. Everything you Need to Know about SaMD from an FDA Perspective

    Opublikowany: 1.03.2021
14. Preparing for Remote and On-Site Inspections and Audits

    Opublikowany: 24.02.2021
15. How does EU MDR impact your Quality Management System?

    Opublikowany: 22.02.2021
16. Virtual Auditing in a Post-COVID World of Digital Compliance

    Opublikowany: 18.02.2021
17. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Opublikowany: 10.02.2021
18. Prioritizing Medical Device Reimbursement During Product Development

    Opublikowany: 4.02.2021
19. 5 Actionable Lessons Learned from the RADx Initiative by NIH

    Opublikowany: 27.01.2021
20. What are the Strategic Priorities for CDRH in 2021?

    Opublikowany: 20.01.2021