R&Q Resources

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

 

 
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Live!

RQM+ Live! #34 — May 6, 2021

Optimizing Technical Documentation to Reduce Notified Body Review Time and..


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RQM+ Live! #33 — April 22, 2021

Types of EU MDR Clinical Evidence Gaps and Best Practice Solutions

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RQM+ Live! #32 — April 8, 2021

What if I'm not ready for EU MDR on May 26, 2021?

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RQM+ Live! #31 — March 25, 2021

Biological Equivalence Demystified

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RQM+ Live! #30 — March 11, 2021

IVD Intended Purpose Statements – Defining for Success

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DEVICE L❤️VE Live! #29 — February 25, 2021

The surprising true cost of submitting non-compliant technical documentation to..

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DEVICE L❤️VE Live! #28 — February 11, 2021

Overcoming Challenges with Integrating PMS, CERs/PERs and Risk Management under..

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

2021 Outlook on FDA Submissions

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

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

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

Is ISO 14971:2019 required under MDR/IVDR?

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

Generating Sufficient Clinical Evidence for IVDs

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

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