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Life Sciences Validation Software Solution

One Validation Solution for All

Res_Q by Sware

Workflow Process Automation for your GxP Systems.

Res_Q automates, integrates, and scales compliance processes across organizations – enabling painless adoption of technologies for life sciences and medical device. With life sciences software solutions like Res_Q, companies can ensure consistency in compliance across their organization and reside in a state of audit readiness. 

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SWR_Icon_Check_2xOne Source

Brings together the key data you need to be always audit ready

SWR_Icon_Water_2xScale Quicker

Launch your quality program and focus on growth milestones

SWR_Icon_Rabbit_2xImplement Faster

Reduces the time it takes for you to validate your computer systems

SWR_Icon_Bank_2xIncrease Value

Increase value by adopting the latest features more quickly

Automate & streamline how you manage the releases of your GxP (and non GxP) systems

Up to 60% less cost on CSV over the life of a system with Res_Q

Immediate Usability is Paramount

At Sware, we have a voracious appetite for velocity and we know that speed matters when it comes to the configuration, implementation, and release management of Res_Q. Life sciences validation software should always be intuitive and never require months of training before use. Res_Q software for life sciences enables teams to accelerate medical device and pharmaceutical software validation, so key resources can spend more time on strategic, innovation-driven efforts.

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, MBA, SVP, Quality Assurance – HUYABIO International

Support to Meet Your Unique Needs

For all life sciences companies, a culture focused on quality is critical not only in your daily activities, but also for the continued success of your organization. With Sware’s services offerings, including medical device and pharmaceutical validation services, we can support you in maintaining a quality-focused culture whether you’re managing a handful – or a plethora – of systems and respective releases.

External Release
Management
Internal Release
Management
Quality
Support
Implementation Validation
& Support
Documents
& Guidance
Managed
Services

The Hottest Life Sciences Platform Features

The team at Sware has carefully curated our feature set to be not only robust but intuitive to use as well. We take great pride in our platform and are excited for you to learn more about what it can do for you. Check out the full set of features and capabilities on the Res_Q platform page.

Validation to Sware by

Res_Q was built to serve the unique, complex requirements around CSV for GxP systems. Leverage our intelligent validation automation platform and our deep compliance expertise to your benefit — reach out today to schedule a no-pressure session  —  We’re here to help you.
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