Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

1. Biocompatibility Nuances and its Impact on Medical Devices

   Gepubliceerd: 7-11-2019
2. How to Make De Novo a Viable Option for your Medical Device

   Gepubliceerd: 7-11-2019
3. Greenlight Guru In the Classroom: A University's Real-world Approach

   Gepubliceerd: 7-11-2019
4. EU MDR: Not All Doom and Gloom

   Gepubliceerd: 7-11-2019
5. Integrating Human Factors into Design Controls to Improve Patient Outcomes

   Gepubliceerd: 7-11-2019
6. Is Your Medical Device Company CAPA Happy?

   Gepubliceerd: 7-11-2019
7. Looking at the Sunset of FDA's Alternative Summary Reporting Program

   Gepubliceerd: 7-11-2019
8. Challenges with MedTech Innovation

   Gepubliceerd: 7-11-2019
9. Design History File Ready Ideation: An Innovative Approach to Product Development

   Gepubliceerd: 7-11-2019
10. Importance of Software Requirements in Product Development

    Gepubliceerd: 7-11-2019
11. 4 Facts That May Surprise You About FDA

    Gepubliceerd: 7-11-2019
12. How General Wellness Devices Have Opened a Pandora's Box of Confusion

    Gepubliceerd: 7-11-2019
13. Regulating Artificial Intelligence and Machine Learning-based Software as a Medical Device

    Gepubliceerd: 7-11-2019
14. Challenges with Pediatric Medical Devices

    Gepubliceerd: 7-11-2019
15. When Should You Start a QMS?

    Gepubliceerd: 7-11-2019
16. Right-sizing your QMS

    Gepubliceerd: 7-11-2019