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 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.
Learn how to move your team away from the old “read and understand” training methods to actually capturing competency. Qualio’s 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 recors.
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.
Our demonstrations are live, so you can get all your questions answered and see how the functionality and
features of the Qualio platform can fit your industry as well as your company’s unique needs.