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GXPNEXT FOR DEVELOPERS

GxPNext: AI-powered validation, right in your application

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Building in GxP spaces should be easier

Navigating GxP presents challenges for developers that want to grow fast and go big in regulated sectors. Solve for success with GxPNext.

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Res_Q Overview (1:48)

From administrative burden to breakthrough innovation

Learn how CDMOs shift skilled teams from rote administration to focused innovation while maintaining compliance excellence. See how Res_Q revolutionizes systems and equipment validation for organizations that refuse to accept the status quo.

90% Faster validation deployment
200+ Validation templates included
100% 21 CFR Part 11 compliant
20+ Years of domain expertise

 

Simplify scoping, execution,
and adoption

  • Scale rapidly with out-of-the-box, flexible technology

  • Seamlessly integrate a GxP validation solution into your SDLC toolkit

  • Optimize your validation strategy for customer use

  • Mitigate the impact of customer audits on your team 

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Achieve total audit-readiness
and peace of mind

  • Automate traceability across requirements and test cases

  • Access audit-ready, customer-accessible document rooms

  • Generate best-in-class GxP validation evidence for customers 

  • Work with the white-glove domain experts at Sware 

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Accelerate time to revenue recognition

  • Automate software release validation workflows

  • Scalable, reusable content validation

  • Reduce your software release validation time by up to 40% 

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Execute customer projects with speed and quality

  • Automate customer validation workflows

  • Standardize and template your delivery process

  • Uncover data-driven insights with project management dashboards

  • Reduce your software implementation validation time by up to 50% 

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SIMPLIFY

Simplify scoping, execution, and adoption

  • Scale rapidly with out-of-the-box, flexible technology

  • Seamlessly integrate a GxP validation solution into your SDLC toolkit

  • Optimize your validation strategy for customer use

  • Mitigate the impact of customer audits on your team 

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ACHIEVE

Achieve total audit-readiness and peace of mind

  • Automate traceability across requirements and test cases

  • Access audit-ready, customer-accessible document rooms

  • Generate best-in-class GxP validation evidence for customers 

  • Work with the white-glove domain experts at Sware

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ACCELERATE

Accelerate time to revenue recognition

  • Automate software release validation workflows

  • Scalable, reusable content validation

  • Reduce your software release validation time by up to 40% 

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EXECUTE

Execute customer projects with speed and quality

  • Automate customer validation workflows

  • Standardize and template your delivery process

  • Uncover data-driven insights with project management dashboards

  • Reduce your software implementation validation time by up to 50% 

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CASE STUDY
How Nuvolo delivered GxP excellence without rebuilding their platform

Learn how this SaaS provider transformed validation from a 7-engineer burden into a strategic differentiator for life sciences customers.

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Our system is completely digitally mapped. As we built out that infrastructure, Sware provided invaluable support by bringing deep industry knowledge, experience, and connections to our project.”

Jason SiegristNuvolo_white
Chief Information Security Officer

Res_Q Features

Features

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Complete validation suite

Deliver comprehensive validation capabilities without the complexity. GxPNext includes everything your customers need: risk assessments, protocol generation, test execution, traceability matrices, and reporting: all built on decades of real-world validation experience.

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Seamless integration

Integrate validation capabilities directly into your existing application architecture. Our flexible APIs and SDKs make it simple to incorporate GxPNext functionality while maintaining your unique user experience and workflow.

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Regulatory compliance built-in

Stay current with evolving regulations automatically. GxPNext includes continuously updated compliance requirements for FDA, EMA, and other global regulatory bodies. Ensure your application always meets current GxP standards.

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Accelerated time to market

Launch validation features in weeks, not years. Pre-built components, templates, and workflows based on industry best practices let you deliver enterprise validation capabilities without extensive development cycles.

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White-label flexibility

Present validation capabilities as native features of your platform. GxPNext supports complete customization of user interfaces, workflows, and branding. Seamlessly integrate with your product vision.

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Scalable cloud architecture

Built for growth from startup to enterprise. Our cloud-native platform scales automatically with your customer base. Reliable performance whether you're serving ten customers or ten thousand.

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Expert partnership

Access validation expertise whenever you need it. Our team provides technical integration support, regulatory guidance, and strategic consultation to ensure your success in the life sciences market.

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Ready to accelerate your development?

Learn how GxPNext can make your life sciences software future-proofed and regulatory-ready.

API-first Architecture

Open API approach unlocks bi-directional data flow that empowers system integrations, migration during onboarding, and more

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Workflow Engine

Configurable workflows to both match your operational requirements and integrate industry best practices

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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

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Intelligent Risk Assessments

Initiate workflows and assign workloads based on risk profile. Res_Q puts quality at the forefront without sacrificing speed

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Full Lifecycle Management

Develop, execute, approve, store, and link to requirements within one centralized paperless validation tool

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Cloud-powered and Secured

Hosted on AWS with separate database instances for each customer environment

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30+ Compliance Modules

Over 30 integrated life sciences applications to accelerate implementation and ongoing release management

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Controlled Auditor Access

Provide inspectors access directly to everything they need within Res_Q to accelerate and pass audits

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One-Centralized-App

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