Res_Q: GxP validation with intelligence
Tap into AI-powered technology backed by deep domain expertise. Fundamentally change your approach to life sciences compliance.
Features
Features
Custom AI assistants handle routine monitoring and flag upcoming milestones.
Turn your validation data into actionable insights that drive better decisions.
Transform any on-screen process into a complete validation script.
Upload assets in any format and watch them become organized and searchable.
Automate risk assessment based on system criticality, eliminating subjectivity and prioritizing workloads.
Connect systems seamlessly for automated data flow and compliance without clicking through interfaces.
Discover how a distributed pharmaceutical research company eliminated validation backlogs and unified 5 industry apps in one digital ecosystem.
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."
Title Here
Pharmaceutical Research Company
Discover how a distributed pharmaceutical research company eliminated validation backlogs and unified 5 industry apps in one digital ecosystem.
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."
Title Here
Pharmaceutical Research Company
Ready to lead the way in life sciences compliance?
Schedule a personalized consultation with our GxP experts.
API-first Architecture
Open API approach unlocks bi-directional data flow that empowers system integrations, migration during onboarding, and more
Workflow Engine
Configurable workflows to both match your operational requirements and integrate industry best practices
One Centralized App
All validation processes are controlled in a single system, serving all areas across the enterprise, including IT, manufacturing, lab systems, and more
Intelligent Risk Assessments
Initiate workflows and assign workloads based on risk profile. Res_Q puts quality at the forefront without sacrificing speed
Full Lifecycle Management
Develop, execute, approve, store, and link to requirements within one centralized paperless validation tool
Cloud-powered and Secured
Hosted on AWS with separate database instances for each customer environment
30+ Compliance Modules
Over 30 integrated life sciences applications to accelerate implementation and ongoing release management
Controlled Auditor Access
Provide inspectors access directly to everything they need within Res_Q to accelerate and pass audits
