Escape Validation Debt Once and For All
Take control of spiraling costs, lost time, and compliance risk with Res_Q
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
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
Puts you on the defensive at crucial moments
Automate, Unify, and Accelerate with Res_Q
The leading-edge life sciences validation platform
Res_Q by Sware automates, unifies, and accelerates all your validation processes, delivering complete peace of mind in a complex compliance environment. With Res_Q, your IT and compliance leaders will spend less time managing disparate GxP systems, avoid slow and error prone paper-based processes, and bridge critical gaps in documentation that complicate communications with auditors.
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
Explore Case Studies
A collection of professional case studies from real clients. See how our customers were rescued from validation debt in their organizations.
"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
Read More"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
Read More"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"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
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.”
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 More"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."
30+ Compliance Modules
Access more than 30 integrated industry-supported applications through Sware's Marketplace to accelerate implementation and automate ongoing compliance.
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 future of life sciences validation and compliance is not so far away. Already, we are seeing life sciences companies rush to integrate AI where possible, while at the same time striving to manage risk with fewer human and material resources available.
Read the WhitepaperLearn how Nuvolo is leveraging a combination of Sware's Res_Q Platform and expert resources to deliver a fully GxP compliant offering to the life sciences industry, enabling Nuvolo and their customers to meet business goals.
Read the case studyManual 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 EbookValidation Debt Stops Here
If your organization is ready to embrace the future of life sciences validation, we’re ready to help.