Medtech Radio - A DeviceAlliance Podcast

Take a ride on DeviceAlliance’s Podcast – Medtech Radio – as we interview some of Orange County, CA best and brightest in our local medical device community

COMMUNITY + COLLABORATION = DEVICEALLIANCE

DeviceAlliance’s podcast ‘Medtech Radio’ is a brand new program addition in 2019 to our Professionals Academy.  As we continue to evolve and grow as an industry, it’s more important than ever we’re continuing to develop ourselves while learning from others experiences.  In this, we will ensure we’re keeping up with the latest technology advances, marketplace trends and opportunities to learn from others experiences and grow in our own professional endeavors.

Medtech Radio podcast’s focus is to highlight the achievements of local Orange County, CA medical device professionals, giving them a platform to share their knowledge and perspective while providing our listeners with an opportunity to learn from and get to know their local colleagues better.

 

LISTEN NOW TO EPISODE #12:


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


EPISODE DESCRIPTION

Jon Speer, Greenlight Guru, DeviceAlliance Podcast MedTech Radio

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.

RESOURCES

Greenlight Guru 

Jon’s LinkedIn

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Episode #12: Coming Soon to Archives

travisDeviceAlliance Podcast – Medtech Radio