Global Medical Device Podcast powered by Greenlight Guru

393 Jaksot

1. Greenlight Guru In the Classroom: A University's Real-world Approach

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

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

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

   Julkaistiin: 7.11.2019
5. Challenges with MedTech Innovation

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

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

   Julkaistiin: 7.11.2019
8. 4 Facts That May Surprise You About FDA

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

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

    Julkaistiin: 7.11.2019
11. Challenges with Pediatric Medical Devices

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

    Julkaistiin: 7.11.2019
13. Right-sizing your QMS

    Julkaistiin: 7.11.2019