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Streamline product development as you scale, including premarket activities, registration, and regulatory compliance.
Achieve FDA 21 CFR Part 820, 21 CFR Part 11, ISO 13485 & 14971 audit-readiness with ease.
Enable real-time feedback capabilities across a distributed workforce to generate revenue sooner.
Avoid having to re-platform in the middle of the crucial startup and scale-up stages.
Track every change and action from beginning to end with fully integrated, closed-loop quality processes.
See how Qualio’s cloud-based document control will eliminate the need for spreadsheets and empower your team to effortlesly create, review, approve, and control documents and records.
Learn how to capture your team's competency with Qualio's training. Our integrated, role-specific training functionality supports in-line assignments as well as tracking of all training activity from within the platform.
Important quality events no longer slip through the cracks. We’ll show you how Qualio can help track quality events; like non-conformances, unapproved deviations, and customer complaints, from creation, to investigation, to root-cause analysis, to CAPA; all the way through to validation of a successful resolution and event closure.
See how Qualio’s cloud-based document control functionality will allow you to finally throw all the spreadsheets away, and empower your team to effortlesly create, review, approve and control documents and records.
See how Qualio can become a single place to manage all audits, suppliers, and change management, so you can see what’s happening across the entire organization in real-time.
Consistently ranked as the quality management platform of choice by medical device manufacturers, therapeutics companices regulated contract service providers.
"Qualio simplifies the approach to effective quality management. The web-based software is intuitive, which greatly reduces the amount of time required for users to come up to speed with a new platform."
"Qualio enabled us to seamlessly work through the ISO 13485:2016 requirements and design errors out of our quality management system. One way Qualio achieves this is to ensure that changes flow through our system and are applied globally."
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