Validation Automation for
Regulated Systems.

Discover why innovative startups and top-tier life sciences leaders alike rely on the Res_Q™ platform. It’s their single source of validation truth to release more products, accelerate implementation, and ensure end-to-end compliance.

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"Validation has always been a time-consuming and disconnected process throughout our organization. With Res_Q we’re aligned and able to manage releases of multiple systems across our enterprise with ease – enabling us to maintain compliance overall.”

Leading Pharma Manufacturer

"The paperwork is bloody daunting… it used to take over 400 hours for each validation pack on a release. Before Sware, we were updating and maintaining Microsoft Word* documents manually, pushing out to DocuSign* and then scanning on the other side so a human can pen-and-ink all this.”

Industry Leading Life Sciences Software Developer

Discover the Res_Q Platform:
Simply a Better Way to Validate

We’ve been there. We know compliant validation is hard work. That’s why we’ve built the platform we wish we always had

Res_Q features pre-built Compliance Modules for intelligent workflow automation, structured risk assessments, and automated testing for more than 30 systems across the life sciences ecosystem. We partner closely with you every step of the way to help you accelerate compliance and deliver speed to users across the enterprise.

Features Built to Fast-Track Validation

Workflow
Builder Drag-&-drop content modules reduce re-work & time to validation

Intelligent Impact
Assessments Eliminates guesswork & re-work for validation tasks

Requirements Specification Manager Create, connect, & execute reqs & test scripts to speed approvals

Validation Overview Smart view of active validation workflows & tasks at-hand

User-Defined Workspace Tailored access to improve team efficiency

Test Script Manager Quickly access script templates & create test scripts to speed validation

Workflow Dashboard
& Reports At-a-glance access & notifications of active workflows speeds throughout times

Enterprise-Level Admin Features One console to serve as validation air-traffic-controller to entire validation lifecycle

Marketplace and
Content Library Growing app store speeds implementations

One Mission. One Platform. One Process.

We’re on a mission to make Computer System Validation (CSV) paperless, seamless, and stressless. That’s why we include a growing marketplace of pre-built compliance modules and ready-to-use templates, SOPs, test scripts, and workflows in an intuitive interface that empowers your teams to accelerate validation end-to-end.

Accelerate Your Digital Transformation

Speed Matters // Res_Q Delivers

Equip your teams to accelerate software validation, drive adoption, and scale faster—profitably.

DEVELOP

Works with
30+ Different Systems

for regulated applications

IMPLEMENT

Up to
30%
Faster

RELEASE

With
80%
Less Effort

Investor Highlight

Behind The Investment: BTR (Now Sware) – Computer System Validation, Automated

We could not be more thrilled to be leading BTR’s $15M Series A with participation from existing investors LRV Health, New Stack, and Jumpstart, and I personally could not be more proud to serve as Board Director on behalf of Insight Partners. Now, post-investment we remain eager to double down on BTR’s rapid commercialization as they continue to shape the future of automated Computer System Validation – this is just the beginning!

// Read the Full Article Here

Exciting News! Boston Technology Research (BTR) is now Sware – Learn More Here

Validation Automation for
Regulated Systems.

Discover why innovative startups and top-tier life sciences leaders alike rely on the Res_Q™ platform. It’s their single source of validation truth to release more products, accelerate implementation, and ensure end-to-end compliance.

Built by Validation Experts for Validation Experts

NEWS BTR ( Now Sware) Raises $15 Million in Series A Round to Transform the Validation Process for Life Sciences // Read More