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GxP validation for leaders who see further

Increase clarity and control with Res_Q: the deeply intelligent, expert-assured platform built for the future of life sciences compliance.

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Res_Q: the intelligent GxP validation platform

Res_Q harnesses agentic AI-powered technology backed by exceptional human support to increase clarity, spur innovation, and ensure quality.

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Data-driven

Create a single source of truth, capture deep insights, and harness the power of AI  
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Transparent

Ensure every decision is explainable, traceable, and reversible  
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Future-proofed

Adapt to industry shifts in real-time and eliminate short-term vendor cycles  
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Data-driven

Create a single source of truth, capture deep insights, and harness the power of AI  
SWR_Transparency_Icon_test

Transparent

Ensure every decision is explainable, traceable, and reversible  
SWR_Transparency_Icon_test

Future-proofed

Adapt to industry shifts in real-time and eliminate short-term vendor cycles  

Res_Q: the intelligent GxP validation platform

Res_Q harnesses agentic AI-powered technology backed by exceptional human support to increase clarity, spur innovation, and ensure quality.

Transform GxP Compliance with AI-Powered Res_Q

Stop losing skilled teams to compliance paperwork. Res_Q's AI-powered platform automates validation, analyzes equipment data, and delivers real-time insights. Ensure your experts focus on high-value work while simplifying change management.

Data-driven to the core
Unify all GxP validation activities through a centralized platform, eliminating data silos, providing a single voice of truth, and enabling advanced analytics
Transparent and change friendly
Manage change with confidence in complex technology ecosystems, ensuring every decision is explainable, traceable, and reversible
Effortlessly future-proofed
Adapt continuously to new regulations and technologies with real-time evolution capabilities, eliminating costly short-term vendor cycles
Data-driven to the core Unify all GxP validation activities through a centralized platform, eliminating data silos, providing a single voice of truth, and enabling advanced analytics
Transparent and change friendly Manage change with confidence in complex technology ecosystems, ensuring every decision is explainable, traceable, and reversible
Effortlessly future-proofed Adapt continuously to new regulations and technologies with real-time evolution capabilities, eliminating costly short-term vendor cycles

From administrative burden to breakthrough innovation

Learn how CDMOs use Res_Q to shift skilled teams from rote administration to focused innovation, freeing capacity while maintaining compliance excellence.

80% Faster validation time
60% Lower lifetime CSV costs
30+ Integrated industry applications
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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

Less Validation Debt, More Peace of Mind

Validation Debt Has You in a Hole

As life sciences companies rapidly adopt new technologies, they incur more and more validation debt: the unpaid, unseen cost of additional release, testing, and GxP requirements. As companies progress through lifecycle stages, validation debt continues to accumulate, affecting timelines and increasing risk.

  • On average, CSV alone adds a minimum 30% or more to overall project costs1

  • The cost of quality assurance affects 12-18% of industry revenue2

  • New FDA regulations factor risk and automation, expecting companies to keep pace3

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1 Gartner 2022 Report, Life Science CIOs: Use Computer Software Assurance to Modernize Your GxP Validation Practice

2 McKinsey and Company Report, The Business Case for Quality

3 U.S. Food & Drug Administration, Computer Software Assurance for Production and Quality System Software

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Validation Debt can increase your organization's compliance risk

The intensifying pace of new software releases and regulatory expectations can make it hard to identify every liability. Take our short, 5-minute survey to gain a better understanding of your overall compliance risk.

Validation Debt can increase your organization's compliance risk

The intensifying pace of new software releases and regulatory expectations can make it hard to identify every liability. Take our short, 5-minute survey to gain a better understanding of your overall compliance risk.

Current Validation Systems:

Require you to be an expert across all GxP systems

Drag teams into slow, error-prone, paper-based processes

Put you on the defensive at crucial moments

Explore Case Studies

A collection of professional case studies from real clients. See how our customers were rescued from validation debt in their organizations.

Case Study - Biopharmaceutical Company
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BUSINESS CHALLENGE:Implementing a Validation Solution to Handle Increased SaaS Releases and Free Up Critical Resources

“Sware is a rare solutions provider that provides both the platform and the people needed to excel at validation, saving us time and money and making our lives considerably easier.”

– Director, Clinical and Development Systems, Biopharmaceutical Company

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BUSINESS CHALLENGE:To Deliver a Modern, Fully Scalable Validation and GxP Compliance Solution to Nuvolo’s Life Sciences Customers

"Today most organizations are using pen and paper which may as well be a stone and chisel.  Our system is completely digitally mapped.  Sware provided invaluable support, bringing deep industry knowledge, experience and connections to our project."

Jason Siegrist, Chief Information Security Officer, Nuvolo

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BUSINESS CHALLENGE:Reduce Validation Bottlenecks, Improve Efficiency and Mitigate Risk Even as Required Validation Volume Grew

"Res_Q has saved us time and resources, reducing validation time by 30-40%. I wholeheartedly recommend Res_Q to fellow industry professionals seeking to enhance their validation processes."

– Sr. Director, IT Business Partner, GxP Systems

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BUSINESS CHALLENGE:An Increasing Burden to Maintain a State of Compliance to Accommodate Growth, a Virtual Organization and Knowledge Gaps

"We have shifted from CSV to CSA and now succeed with less documentation and more critical thinking. The difference pre- and post-  Res_Q is simply night and day, we have accelerated our validation time by 75%!"

Read More
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BUSINESS CHALLENGE:Existing Computer System Validation Couldn't Ensure GxP Across the Digital Ecosystem

"The time to execute validation workstreams went from days to hours with the implementation of Res_Q. We now have a proactive posture when it comes to cost and risk management. Res_Q is now a fundamental part of our bigger technology and compliance picture."

– Senior Director, Development Informatics

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Explore Case Studies B

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Explore Case Studies C

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Trusted by life sciences leaders

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“Working with Sware has accelerated our ability to bring trusted, validated AI solutions to life sciences companies. Their Res_Q platform seamlessly integrates with Salesforce Life Sciences Cloud, giving our customers the confidence to adopt AI-powered workflows while ensuring full GxP compliance."

Frank D   |   SVP and General Manager

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"We highly recommend Res_Q for its simplicity and effectiveness. [The] software is exceptionally user-friendly, enabling streamlined audits through controlled auditor access. All validation activities are consolidated within a single app, ensuring consistency and transparency. The prebuilt templates simplify implementation and promote uniform validation processes."

Jim H   |   Director of Quality

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"Res_Q has transformed our ability to manage CSV/CSA deliverables electronically, supporting our workforce both in-office and remotely. Its intuitive design simplifies configuration and evolves with our needs, while enabling seamless traceability by connecting information previously stored in paper documents.” 

Senior Director, Head of IT   |    Molecular Medicine Company

"Sware is an extremely responsive organisation, managing our entire relationship from initial discussions through final validation deliverables, which they provided quickly and professionally.” 

Steven B  |   Chief Data Officer

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"Frequent releases of software (like Veeva Vault® and DocuSign®) can include major changes and keeping up with documenting the configuration changes can become a full-time job. With Sware’s paperless Res_Q platform, we can easily navigate electronic change management and change control processes."

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Blake Jensen, MBASVP, Quality Assurance, HUYABIO International

"Res_Q has saved us significant time and resources, reducing validation time by 30-40%. I wholeheartedly recommend it to industry professionals enhancing their validation practices."

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Senior DirectorIT Business Partner, GxP Systems, Biotechnology Company

"Sware is a rare solutions provider that provides both the platform and the people needed to excel at validation, saving us time and money and making our lives considerably easier."

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DirectorClinical and Development Systems, Biopharmaceutical Company

"[Pending approval]Our partnership with Sware offers Salesforce Life Sciences Cloud users a compelling way to embed robust, efficient, and scalable GxP validation directly into their cloud environment. This helps our customers focus on groundbreaking work instead of compliance logistics. Additionally, Sware doesn't just provide a platform; their leadership team has spent decades solving complex life sciences compliance challenges and building solutions with industry-wide impact."

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Frank DSalesforce

"Frequent releases of software (like Veeva Vault® and DocuSign®) can include major changes and keeping up with documenting the configuration changes can become a full-time job. With Sware’s paperless Res_Q platform, we can easily navigate electronic change management and change control processes."

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Blake Jensen, MBASVP, Quality Assurance, HUYABIO International

"Res_Q has saved us significant time and resources, reducing validation time by 30-40%. I wholeheartedly recommend it to industry professionals enhancing their validation practices."

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Senior DirectorIT Business Partner, GxP Systems, Biotechnology Company

"Sware is a rare solutions provider that provides both the platform and the people needed to excel at validation, saving us time and money and making our lives considerably easier."

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DirectorClinical and Development Systems, Biopharmaceutical Company

Integrated with your compliance ecosystem

Seamlessly connect with 30+ compliance modules and industry-leading platforms through our comprehensive, API-based system.

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Insights 

Our library of openly available resources is designed to equip you with the knowledge you need to tackle validation challenges effectively.

Integrated with your compliance ecosystem

Seamlessly connect with 30+ compliance modules and industry-leading platforms through our comprehensive, API-based system.

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Take the next step

Ready to implement a more intelligent approach to GxP validation? Schedule a consultation with a Sware expert to explore how Res_Q can meet your unique needs.

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Take the next step

Talk to a Sware expert to see how you can forge a new path in life sciences compliance.