R&Q Resources

Upcoming and on-demand education, commentary from thought leaders, Q&A features, and more.


 In the midst of the coronavirus pandemic and reduced travel/networking, please remember our Resources page offers the latest education, training, and industry information from R&Q. 


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Live!

DEVICE L❤️VE Live! #16 — August 27, 2020

Creating Performance Evaluation Plans and Reports under the IVDR


Live!

DEVICE L❤️VE Live! #15 — August 13, 2020

When to use the FDA Q-Submission (Pre-Sub) Program

Live!

DEVICE L❤️VE Live! #14 — July 30, 2020

Is your device a Well-Established Technology (WET) under EU MDR?

Live!

DEVICE L❤️VE Live! #13 — July 16, 2020

Is this software application a medical device?

Live!

DEVICE L❤️VE Live! #12 — July 2, 2020

Tips and Tricks for a Smooth 510(k) Process

News, CER, EU MDR, Live!

State of the Art (SOTA) Part I: What is a State ...

You have been reviewing the 4th revision of the European Commission’s..

Live!

DEVICE L❤️VE Live! #11 — June 25, 2020

I don't have clinical data for my device. What are my options for fulfilling..

Live!

DEVICE L❤️VE Live! #10 — June 18, 2020

Transition to IVDR: How far along should we be?

Live!

DEVICE L❤️VE Live! #9 — June 11, 2020

Experiences with the FDA 3rd Party 510(k) Review Program

Live!

DEVICE L❤️VE Live! #8 — June 4, 2020

FDA Trends: Inspections and Submissions

Live!

DEVICE L❤️VE Live! #7 — 5/28/20

Getting Legacy Device Risk Files Ready for EU MDR / ISO 14971:2019

Live!

DEVICE L❤️VE Live! #6 — 5/21/20

PMCF Process in Action: Best Practices for MDR Compliance