Global Medical Device Podcast powered by Greenlight Guru

398 Episodes

1. Knowing vs. Doing as Medical Device Professionals

   Published: 4/20/2021
2. Pivoting Operations to Meet PPE Demand during Pandemic

   Published: 4/14/2021
3. Pros & Cons of Being a Physician turned MedTech Inventor

   Published: 4/13/2021
4. 3 Systems of Risk for Medical Devices from FDA

   Published: 4/8/2021
5. Quality Management for IVD Devices vs Medical Devices

   Published: 4/5/2021
6. Understanding the Investigational Device Exemption (IDE) Process

   Published: 3/31/2021
7. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

   Published: 3/30/2021
8. Why the PMA Process is so Dreaded by Manufacturers in the US Market

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

   Published: 3/24/2021
10. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

    Published: 3/21/2021
11. Meet a Guru: Sara Adams

    Published: 3/17/2021
12. Building a Startup in the MedTech Industry

    Published: 3/10/2021
13. Meet a Guru: Karen Schuyler

    Published: 3/8/2021
14. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Published: 3/4/2021
15. Everything you Need to Know about SaMD from an FDA Perspective

    Published: 3/1/2021
16. Preparing for Remote and On-Site Inspections and Audits

    Published: 2/24/2021
17. How does EU MDR impact your Quality Management System?

    Published: 2/22/2021
18. Virtual Auditing in a Post-COVID World of Digital Compliance

    Published: 2/18/2021
19. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Published: 2/10/2021
20. Prioritizing Medical Device Reimbursement During Product Development

    Published: 2/4/2021