Skip to content
SWR_Validation-Debt-Ladder-Hero_final_16-9_web

Escape Validation Debt
Once and For All

Take control of spiraling costs, lost time,
and compliance risk with Res_Q

 

Validation-Debt-Compounds-Over-Time_Illustration_1200x700

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

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.

SWR_Icon_Automate

Automate
release testing and GxP validation

SWR_Icon_Unify

Unify
validation processes in one app

SWR_Icon_Accelerate

Accelerate
validation time by up to 80%

SWR_Icon_Ensure

Ensure
transparency and audit readiness

Less Validation Debt, More Peace of Mind

"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."

Blake-Jensen_Huyabio-International_headshot
Blake Jensen, MBASVP, Quality Assurance, HUYABIO International

30+ industry accelerators

Access more than 30 integrated industry-supported applications through Sware's Marketplace to accelerate implementation and automate ongoing compliance.

Compliance-Modules-Logos
30+ Industry-supported Applications
60% Lower Lifetime CSV Costs
250+ Companies Served

Insights 

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

Insights 

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

Validation Debt Stops Here

If your organization is ready to embrace the future of life sciences validation, we’re ready to help.