R&Q Resources

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

 

 
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Live!

DEVICE L❤️VE Live! #27 — January 28, 2021

2021 Outlook on FDA Submissions


Live!

DEVICE L❤️VE Live! #26 — January 14, 2021

What is the Biggest EU MDR or IVDR Question You Need to be Answered?

Live!

DEVICE L❤️VE Live! #25 — 17 December, 2020

Is ISO 14971:2019 required under MDR/IVDR?

Live!

DEVICE L❤️VE Live! #24 — 3 December, 2020

Generating Sufficient Clinical Evidence for IVDs

Live!

DEVICE L❤️VE Live! #23 — 19 November, 2020

Make real world evidence work for you: How to leverage real world data in the..

Live!

DEVICE L❤️VE Live! #22 — 5 November, 2020

Summary of Safety and Clinical Performance

Live!

DEVICE L❤️VE Live! #21 — 22 October, 2020

Avoid Audit Findings! Collecting Relevant Data for PMCF Surveys

Live!

DEVICE L❤️VE Live! #20 — 8 October, 2020

Commercializing Medical Devices in a Post-Brexit World

Live!

DEVICE L❤️VE Live! #19 — 24 September, 2020

The most popular PMCF and PMPF questions from our clients

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Ranked: The most popular on-demand panel ...

Note: A version of this post was initially published for the flagship online..

Live!

DEVICE L❤️VE Live! #17 — September 10, 2020

Periodic Safety Update Report: How do you write it without guidance?

Live!

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

Creating Performance Evaluation Plans and Reports under the IVDR