Global Medical Device Podcast powered by Greenlight Guru

398 Jaksot

1. Knowing vs. Doing as Medical Device Professionals

   Julkaistiin: 20.4.2021
2. Pivoting Operations to Meet PPE Demand during Pandemic

   Julkaistiin: 14.4.2021
3. Pros & Cons of Being a Physician turned MedTech Inventor

   Julkaistiin: 13.4.2021
4. 3 Systems of Risk for Medical Devices from FDA

   Julkaistiin: 8.4.2021
5. Quality Management for IVD Devices vs Medical Devices

   Julkaistiin: 5.4.2021
6. Understanding the Investigational Device Exemption (IDE) Process

   Julkaistiin: 31.3.2021
7. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

   Julkaistiin: 30.3.2021
8. Why the PMA Process is so Dreaded by Manufacturers in the US Market

   Julkaistiin: 25.3.2021
9. Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

   Julkaistiin: 24.3.2021
10. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

    Julkaistiin: 21.3.2021
11. Meet a Guru: Sara Adams

    Julkaistiin: 17.3.2021
12. Building a Startup in the MedTech Industry

    Julkaistiin: 10.3.2021
13. Meet a Guru: Karen Schuyler

    Julkaistiin: 8.3.2021
14. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Julkaistiin: 4.3.2021
15. Everything you Need to Know about SaMD from an FDA Perspective

    Julkaistiin: 1.3.2021
16. Preparing for Remote and On-Site Inspections and Audits

    Julkaistiin: 24.2.2021
17. How does EU MDR impact your Quality Management System?

    Julkaistiin: 22.2.2021
18. Virtual Auditing in a Post-COVID World of Digital Compliance

    Julkaistiin: 18.2.2021
19. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Julkaistiin: 10.2.2021
20. Prioritizing Medical Device Reimbursement During Product Development

    Julkaistiin: 4.2.2021