31 min listen
Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View
FromGlobal Medical Device Podcast powered by Greenlight Guru
Inside Look into ISO 14971:2019 & ISO TR 24971:2020 from the Author's Point of View
FromGlobal Medical Device Podcast powered by Greenlight Guru
ratings:
Length:
40 minutes
Released:
Feb 10, 2021
Format:
Podcast episode
Description
Keeping a constant pulse on current medical device industry standards for risk management, like ISO 14971:2019 and its companion documents, while also adhering to the recommended guidelines is one of the most important things a medical device company can do to be successful.
In this episode of the Global Medical Device Podcast, Jon Speer talks to Ed Bills, risk management consultant and technical committee member of the working group for ISO 14971:2019 and ISO TR 24971:2020, who shares key insights from his work developing the latest version of the international risk standard and offers recommendations for companies that will help strengthen their product risk management practices.
In this episode of the Global Medical Device Podcast, Jon Speer talks to Ed Bills, risk management consultant and technical committee member of the working group for ISO 14971:2019 and ISO TR 24971:2020, who shares key insights from his work developing the latest version of the international risk standard and offers recommendations for companies that will help strengthen their product risk management practices.
Released:
Feb 10, 2021
Format:
Podcast episode
Titles in the series (100)
How to Properly Use the FDA Pre-Submission Process and Why It's So Important with Mike Drues: In order to get your medical device to market, you will need to know about pre-submission and the pre-submission process. The FDA is trying to get the safest medical devices out there. The most common reasons that the FDA makes rejections is within t... by Global Medical Device Podcast powered by Greenlight Guru