
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.
Data-driven
Create a single source of truth, capture deep insights, and harness the power of AITransparent
Ensure every decision is explainable, traceable, and reversibleFuture-proofed
Adapt to industry shifts in real-time and eliminate short-term vendor cyclesData-driven
Create a single source of truth, capture deep insights, and harness the power of AITransparent
Ensure every decision is explainable, traceable, and reversibleFuture-proofed
Adapt to industry shifts in real-time and eliminate short-term vendor cyclesRes_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.
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.
Automate
release testing and GxP validation
Unify
validation processes in one app
Accelerate
validation time by up to 80%
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.
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On average, CSV alone adds a minimum 30% or more to overall project costs1
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The cost of quality assurance affects 12-18% of industry revenue2
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New FDA regulations factor risk and automation, expecting companies to keep pace3

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
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.

“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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"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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"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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"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%!"
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"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
Read MoreExplore Case Studies B
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"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.”
Read MoreExplore Case Studies C
Description. Lorem ipsum dolor sit amet, consetetur sadipscing elitr, sed diam nonumy eirmod tempor invidunt ut labore et

"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.”
"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.”
Read MoreResources to accelerate your success
Resources to accelerate your success
Trusted by life sciences leaders
















“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
"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
"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
"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."

"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."
"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."
"[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."
"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."

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

Insights
Our library of openly available resources is designed to equip you with the knowledge you need to tackle validation challenges effectively.
Featured Resources
The convergence of AI and Quality Management marks a paradigm shift in how Life Sciences organizations meet their GxP obligations. Examine key challenges—from compliance complexities and validation demands to talent shortages and risk management concerns.
Read the WhitepaperAs the life sciences landscape rapidly evolves, technology adoption demands agile validation methods to maintain GxP compliance. Learn how organizations can shift from project-based validation to a process-driven approach, integrating validation into their Quality Management System.
Read the WhitepaperManual computer software validation processes cost life sciences organizations up to 30% in additional project budget. As companies struggle to keep up with a surge of app and software integrations, they incur validation debt: the mounting cost of stretched resources, blanket testing, and missed GxP requirements.
Download the EbookIntegrated with your compliance ecosystem
Seamlessly connect with 30+ compliance modules and industry-leading platforms through our comprehensive, API-based system.

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.
