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Transform Your GxP Validation Process

Learn more about the data-driven platform that unifies and simplifies every aspect of GxP validation and change management

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Transform Your GxP Validation Process

Experience the data-driven platform that unifies and simplifies every aspect of validation and change management

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Download Our eBook

Res_Q by Sware eliminates traditional validation bottlenecks by centralizing operations, automating workflows, and ensuring audit-readiness—all while reducing validation time by up to 80%. Download our eBook “Rescue your Organization from Validation Debt” and learn more.

Why Choose Res_Q?

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Automate
release, testing, and GxP validation

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Unify
validation processes in one app

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Accelerate
validation time by up to 80%

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Ensure
transparency and audit readiness

Powerful Features That Deliver Results

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API-first Architecture

Connect your systems seamlessly with bi-directional data flow that empowers integrations and streamlines migrations.

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Intelligent Risk Assessments

Prioritize quality without sacrificing speed using risk profiles that initiate workflows and assign workloads automatically.

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One Centralized App

Control all validation processes in a single system serving IT, manufacturing, lab systems, and more across your enterprise.

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Full Lifecycle Management

Develop, execute, approve, store, and link to requirements within one paperless validation environment.

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Workflow Engine

Configure workflows that match your operational requirements while integrating industry best practices.

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30+ Compliance Modules

Accelerate implementation with over 30 integrated life sciences applications for streamlined release management.

What Our Customers Say

“Res_Q has saved us significant time and resources, allowing us to focus on core business objectives and reducing validation time by 30-40%. I wholeheartedly recommend Res_Q to fellow industry professionals seeking to enhance their validation practices.” 
Senior Director and IT Business Partner, GxP SystemsBiotechnology Company
“Validation workstreams that weren’t in Res_Q took days. Those same workstreams, once moved into the Res_Q system, take hours. It has helped us move from a reactive to proactive posture when it comes to cost and risk management and is a fundamental part of our bigger technology and compliance picture.”
Senior Director, Development InformaticsMolecular Medicine Company
“Sware is a rare solutions provider in that it provides both disruptive technology and a team of true functional experts. Sware provides both the platform and people needed to excel at validation, saving us time and money and making our lives considerably easier.” 
Director, Clinical and Development SystemsBiopharmaceutical Company