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Jon Speer: Bringing Safe Products to Market Fast | Ep.12

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Manage episode 280098492 series 2839727
Content provided by Creighton Chaney. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Creighton Chaney or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
How does one take a medical device idea on a napkin to a 510k approval to market release as efficiently as possible? How does one manage risk to drive the safety and quality of products and processes, while striving to be first in a innovative market? How does one change their company’s focus from simply meeting regulations to building quality into their processes as a differentiator?

How does one understand and stay ahead of the FDA and EU changing quality regulations as leaders instead of followers? In this episode of DeviceAlliance’s Medtech Radio, we speak with Founder of Greenlight Guru, Jon Speer. Join us as he shares his deep insights in the differences that help medical devices get to market faster with less risk. Greenlight Guru is the only quality management software platform designed specifically for medical devices companies. The platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more.

  continue reading

57 episodes

Artwork
iconShare
 
Manage episode 280098492 series 2839727
Content provided by Creighton Chaney. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Creighton Chaney or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
How does one take a medical device idea on a napkin to a 510k approval to market release as efficiently as possible? How does one manage risk to drive the safety and quality of products and processes, while striving to be first in a innovative market? How does one change their company’s focus from simply meeting regulations to building quality into their processes as a differentiator?

How does one understand and stay ahead of the FDA and EU changing quality regulations as leaders instead of followers? In this episode of DeviceAlliance’s Medtech Radio, we speak with Founder of Greenlight Guru, Jon Speer. Join us as he shares his deep insights in the differences that help medical devices get to market faster with less risk. Greenlight Guru is the only quality management software platform designed specifically for medical devices companies. The platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more.

  continue reading

57 episodes

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