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Events, Podcasts, and Webinars

Stay connected with RookQS across the MedTech community, from live events to on-demand insights.

On-Demand Webinars

Check out our webinars to get actionable insights in the MedTech community. Click below to see the full list of on-demand webinars.


Upcoming Events

Sept. 15 & 16

Houston MedTech Oktoberfest

Jacob Carlisle will be representing RookQS at this year's celebration of MedTech innovation, connection, and community. If you're navigating QMS, regulatory submissions, SaMD, or audit readiness, grab a stein and a few minutes with Jacob to talk through how RQS can help.

Book time with Jacob.

Sept. 18 - 20

HRX 2026

Kyle Rose will be representing RookQS at HRX in Atlanta, where the boldest minds in cardiac electrophysiology and cardiovascular innovation come together. If you're building the next breakthrough in cardiac care and need a quality and regulatory partner who can keep pace, connect with Kyle to learn how RQS can help you get there faster.

Book time with Kyle.

Sept. 28 - Oct. 1

LSI Europe

Kyle Rose will be representing RookQS at one of the global medtech community's premier gatherings where top executives, innovative startups, and active investors come together to shape the future of the industry. If you're a founder, executive, or investor looking for a quality and regulatory partner who understands the demands of scaling a medtech company, connect with Kyle to see how RookQS can support your journey.

Book time with Kyle.

Oct. 18-21

AdvaMed's The MedTech Conference

Kyle Rose, Jacob Carlisle, and Joseph McGonnigal will all be representing RookQS at the industry's biggest stage, where medtech innovators, investors, and leaders gather to shape the future of healthcare. Whether you're navigating QMS, regulatory submissions, SaMD, or audit readiness, our team is ready to connect.

Find us in the partnering app and let's set up time to talk!

Podcast Appearances

FDA’s ISO 13485 Transition Plan … What Does it Mean for Your Medtech’s Quality Plan?
April 27, 2022
LISTEN NOW In this episode of the Project Medtech Podcast, Rook Founder/President Kyle Rose and Duane Mancini discuss in detail the FDA’s ISO-13485 transition plan, when it was announced, what it looks like, the differences 21 CFR Part 820 vs....
Tips, Tricks, and Best Practices for Complying with ISO13485:2016
November 05, 2020
LISTEN NOW When it comes to 13485-2016, are you scrambling to meet requirements? Are you trying to figure out the how, what, or when regarding its timeline? Or, maybe you just don’t know what you need to do. You are not alone because a lot of...
What are the regulatory expectations for Software as a Medical Device (SaMD)?
November 05, 2020
LISTEN NOW This podcast was hosted by Andrew Wu, the Software Consultant of Rook Quality Systems. You will find this podcast helpful for understanding how Rook helps SaMD companies ensure that their documentation, platform, and systems they...
Implementing Changes to SaMD under new EU MDR
October 11, 2020
LISTEN NOW Hosted by Andrew Wu of Rook Quality Systems, this podcast will help you understand changes imposed on SaMD under new EU MDR. SaMD manufacturers will benefit from clarifications on qualification and classification changes and action...

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