Watch the webinar recording: everything you need to know about the FDA QMSR

We partnered with global auditing giant DQS for a deep-dive discussion of the FDA's latest medical device regulation.

Catch the full webinar recording now!

 

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Watch the recording now

What you'll learn

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Every change from the old FDA 21 CFR 820 Quality System Regulation (QSR)

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What you need to do to get compliant after February 2, 2026

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The processes and QMS ingredients you'll need to add and update

5-star reviews on Capterra, G2, Getapp, and SoftwareAdvice
Consistently ranked as the quality management platform of choice by medical device
manufacturers, therapeutics companies regulated contract service providers.
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I find Qualio a brilliant software.

Pamela

Director of Clinical Development

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All requires aspects of a QMS are present in Qualio.

Drew

Director of Quality

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It is very user friendly and intuitive.

Paul

Med Device Account Manager

Qualio: loved and trusted by 650+ life science companies worldwide

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QUALIO CUSTOMERS ENJOY...

30% faster quality processes
90% less quality admin
140% increase in product release speed
5x faster external audits

And more.

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Exceptionally great, easy to access SOPs.

Elias

Medical Technologist

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Easy to locate and review documents.

Mallory

Clinical Trial Associate