Res_Q is a platform that streamlines computer system validation workflows and eases the distibution of release content between regulated software producers and software consumers, providing bi-directional visibility and traceability.
Today, leading life sciences organizations use Res_Q to manage all things validation across the enterprise. Leading software vendors use Res_Q to validate their products and software releases. Res_Q by Sware is an extremely easy-to-use and ever audit-ready solution for automating validation across the software lifecycle for GxP systems. Res_Q automates, integrates, and scales compliance processes across organizations, enabling painless adoption of technologies for life sciences and medical device companies.
Using Res_Q, companies perform structured risk assessment, automate workflows, and execute 21 CFR Part 11 compliant signatures in one, simple platform. With Res_Q, companies can ensure consistency in compliance across their organization and have an authoritative system of record to ensure audit readiness.
For early stage life sciences companies just beginning to use GxP software, Sware offers the Res_Q Quality Startup Bundle. Included in this validation as a services (VaaS) accelerator package are Res_Q licenses, a core set of computer software assurance (CSA) standard operating procedures (SOPs) built by industry validation experts, and a Sware built compliance module.
Res_Q for SMB and Enterprise is available through private offers. Please email us at marketplace@sware.com to learn more.
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Pricing is based on the duration and terms of your contract with the vendor. This entitles you to a specified quantity of use for the contract duration. If you choose not to renew or replace your contract before it ends, access to these entitlements will expire.
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This listing offers one pricing option: Res_Q Quality Startup, sold under a contract by the unit. It is packaged as Validation as a Service for life sciences startups. You buy a set quantity of units for the committed term, so cost scales with the number of units you select. There are no separate tiers or add-on dimensions to combine. The unit-based structure lets you match your purchase to the scope of GxP validation work your team needs to manage.
Top-of-mind questions for buyers
What counts as one unit for billing under the Res_Q Quality Startup contract?
The pricing table sells Res_Q Quality Startup by the unit under a contract. The marketplace data does not define what one unit maps to in concrete terms, such as a validated system, a user seat, or a validation project. Contact the vendor to confirm how units are counted for your use case.
What validation capabilities does the Res_Q Quality Startup package cover?
Res_Q is a GxP validation platform for life sciences teams. It supports validation across clinical, laboratory, manufacturing, and AI systems. Features include risk-based scoring, automated monitoring, dashboards, video-to-script capture, and audit-trailed connections to common IT and testing tools. This package targets life sciences startups.
How does my cost change if my validation workload grows?
Cost scales with the number of units you buy for the committed term. You select a set quantity upfront, so adding more validation scope means purchasing more units. There are no separate tiers or add-on dimensions. The marketplace data does not describe automatic scaling, so contact the vendor about mid-term increases.
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