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RES_Q PLATFORM

Res_Q: GxP validation with intelligence

Tap into AI-powered technology backed by deep domain expertise. Fundamentally change your approach to life sciences compliance.

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VIDEO

From administrative burden to process accelerator

See how contract development manufacturing organizations (CDMOs) shift teams from administration to innovation.

80% Faster validation time
60% Lower lifetime CSV costs
30+ Integrated applications
100% Traceable and defensible

Features

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Agentic AI capabilities

Custom AI assistants handle routine monitoring and flag upcoming milestones.

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Smart dashboards & analytics

Turn your validation data into actionable insights that drive better decisions.

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Video-to-script capture

Transform any on-screen process into a complete validation script.

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Instant asset processing

Upload assets in any format and watch them become organized and searchable.

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Automated risk scoring

Automate risk assessment based on system criticality, eliminating subjectivity and prioritizing workloads.

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Open API architecture

Connect systems seamlessly for automated data flow and compliance without clicking through interfaces.

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CASE STUDY
A virtual quality team achieves 75% faster validation

Discover how a distributed pharmaceutical research company eliminated validation backlogs and unified 5 industry apps in one digital ecosystem.

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The difference pre- and post-Res_Q is simply night and day. What used to take us weeks or months now takes us days or weeks."

Senior Director, IT Business Partner, GXP Systems
Pharmaceutical Research Company

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Ready to lead the way in life sciences compliance?

Schedule a personalized consultation with our GxP experts.