One Validation
Platform for All
Res_Q is an extremely easy-to-use solution for managing all your GxP systems.
Purpose-built, cost-efficient, and always audit-ready
Res_Q: Workflow Process Automation for GxP Systems
Res_Q automates, integrates, and scales compliance processes across organizations – enabling painless adoption of technologies for life sciences and medical device. With Res_Q, companies can ensure consistency in compliance across their organization and reside in a state of audit readiness.


Bring together the key data you need to be always audit-ready

Launch your quality program and focus on growth milestones

Reduce the time it takes to
adopt solutions

Deliver more releases while decreasing the burden on customers
With Res_Q, we’re aligned and able to manage releases of multiple systems across our enterprise with ease – enabling us to maintain compliance overall.
– Leading Pharma Manufacturer
Pre-built Compliance Modules
Providing a starting point from which to validate, Sware offers pre-built compliance modules for more than 30 life sciences systems. These modules provide content you can easily edit, accelerating your compliance and speeding up implementation to get your team up and running quickly.

Built by Validation Experts
We're on a mission to make validation paperless, seamless, and stressless. That's why we include a growing marketplace of pre-built compliance modules and ready-to-use templates, SOPs, test scripts, and workflows in an intuitive interface that empowers your teams to accelerate validation end-to-end.
Implementations
Upgrades