Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. Biocompatibility Nuances and its Impact on Medical Devices

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

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

   Published: 11/7/2019
4. EU MDR: Not All Doom and Gloom

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

   Published: 11/7/2019
6. Is Your Medical Device Company CAPA Happy?

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

   Published: 11/7/2019
8. Challenges with MedTech Innovation

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

   Published: 11/7/2019
10. Importance of Software Requirements in Product Development

    Published: 11/7/2019
11. 4 Facts That May Surprise You About FDA

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

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

    Published: 11/7/2019
14. Challenges with Pediatric Medical Devices

    Published: 11/7/2019
15. When Should You Start a QMS?

    Published: 11/7/2019
16. Right-sizing your QMS

    Published: 11/7/2019