Podcast: Listen – Medtronic Exec Highlights Ethylene Oxide Standards At First Day Of FDA EtO Meeting

Medtronic’s director of quality sterilization and microbiology, Phil Cogdill, sat down with Medtech Insight to talk about setting new ethylene oxide (EtO) standards and what his takeaways were from the first day of a US FDA meeting to understand how to mitigate potential product shortages from closures of EtO sterilization facilities. Check out our podcast here.

MT1911_Cogdill.jpg
Medtronic’s Phil Cogdill brought a sterilized oxygenator used in cardiac surgery to a US agency meeting on ethylene oxide (EtO) to show experts how difficult it is to clean such lifesaving products • Source: Ferdous Al-Faruque

Phil Cogdill, director of quality sterilization and microbiology at Medtronic, spoke before a panel of experts about the importance of setting new ethylene oxide (EtO) standards to clean medical devices. While it may take years for such standards to fully go into effect, he and other experts have already rolled up their sleeves to get the job done.

The US Food and Drug Administration kicked off a two-day meeting on 6-7 November in Gaithersburg, MD, to discuss how...

Medtech Insight Podcast

Keep up with the top medtech business and regulatory news.

Medtech Insight brings you interviews and analysis, on the go.

More from Regulation

More from Policy & Regulation