Global Medical Device Podcast powered by Greenlight Guru

398 Jaksot

1. The 100th Episode: A Few of My Favorite Moments

   Julkaistiin: 7.11.2019
2. Live Atlanta True Quality Roadshow Panel: The Changing Quality & Regulatory Paradigm

   Julkaistiin: 7.11.2019
3. Biocompatibility Nuances and its Impact on Medical Devices

   Julkaistiin: 7.11.2019
4. How to Make De Novo a Viable Option for your Medical Device

   Julkaistiin: 7.11.2019
5. Greenlight Guru In the Classroom: A University's Real-world Approach

   Julkaistiin: 7.11.2019
6. EU MDR: Not All Doom and Gloom

   Julkaistiin: 7.11.2019
7. Integrating Human Factors into Design Controls to Improve Patient Outcomes

   Julkaistiin: 7.11.2019
8. Is Your Medical Device Company CAPA Happy?

   Julkaistiin: 7.11.2019
9. Looking at the Sunset of FDA's Alternative Summary Reporting Program

   Julkaistiin: 7.11.2019
10. Challenges with MedTech Innovation

    Julkaistiin: 7.11.2019
11. Design History File Ready Ideation: An Innovative Approach to Product Development

    Julkaistiin: 7.11.2019
12. Importance of Software Requirements in Product Development

    Julkaistiin: 7.11.2019
13. 4 Facts That May Surprise You About FDA

    Julkaistiin: 7.11.2019
14. Regulating Artificial Intelligence and Machine Learning-based Software as a Medical Device

    Julkaistiin: 7.11.2019
15. How General Wellness Devices Have Opened a Pandora's Box of Confusion

    Julkaistiin: 7.11.2019
16. Challenges with Pediatric Medical Devices

    Julkaistiin: 7.11.2019
17. When Should You Start a QMS?

    Julkaistiin: 7.11.2019
18. Right-sizing your QMS

    Julkaistiin: 7.11.2019