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.