Global Medical Device Podcast powered by Greenlight Guru

416 Episodio

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

   Pubblicato: 13/04/2021
2. 3 Systems of Risk for Medical Devices from FDA

   Pubblicato: 07/04/2021
3. Quality Management for IVD Devices vs Medical Devices

   Pubblicato: 05/04/2021
4. Understanding the Investigational Device Exemption (IDE) Process

   Pubblicato: 31/03/2021
5. Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

   Pubblicato: 30/03/2021
6. Why the PMA Process is so Dreaded by Manufacturers in the US Market

   Pubblicato: 25/03/2021
7. Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

   Pubblicato: 24/03/2021
8. What is the Safer Technologies Program (STeP) and Can Your Device Use It?

   Pubblicato: 21/03/2021
9. Meet a Guru: Sara Adams

   Pubblicato: 17/03/2021
10. Building a Startup in the MedTech Industry

    Pubblicato: 10/03/2021
11. Meet a Guru: Karen Schuyler

    Pubblicato: 08/03/2021
12. Visualizing a Medical Device through Illustrations, Animations, and other Artwork

    Pubblicato: 04/03/2021
13. Everything you Need to Know about SaMD from an FDA Perspective

    Pubblicato: 01/03/2021
14. Preparing for Remote and On-Site Inspections and Audits

    Pubblicato: 24/02/2021
15. How does EU MDR impact your Quality Management System?

    Pubblicato: 22/02/2021
16. Virtual Auditing in a Post-COVID World of Digital Compliance

    Pubblicato: 18/02/2021
17. Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View

    Pubblicato: 10/02/2021
18. Prioritizing Medical Device Reimbursement During Product Development

    Pubblicato: 04/02/2021
19. 5 Actionable Lessons Learned from the RADx Initiative by NIH

    Pubblicato: 27/01/2021
20. What are the Strategic Priorities for CDRH in 2021?

    Pubblicato: 20/01/2021