Audience

Pharmaceutical companies, biotechnology organizations, contract development and manufacturing organizations (CDMOs), clinical research organizations, life sciences IT teams, quality assurance professionals, validation engineers, regulatory compliance managers, and computer system validation specialists seeking AI-powered GxP validation, automated compliance workflows, risk assessment, and audit-ready documentation

About Res_Q

Res_Q is an AI-powered GxP validation and compliance management platform developed by Sware for organizations operating in regulated life sciences environments. The software centralizes computerized system validation, documentation, risk assessments, testing, and approval workflows within a cloud-based platform. Its agentic AI capabilities automate routine validation activities, monitor progress, and identify milestones requiring human attention. Res_Q provides intelligent risk scoring, automated document processing, video-to-test-script generation, and dashboards for analyzing validation activities. The platform supports Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and AI system validation requirements. Integration capabilities connect Res_Q with enterprise applications, testing tools, and quality management systems while maintaining traceable records and audit trails.

Integrations

API:
Yes, Res_Q offers API access

Ratings/Reviews

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Company Information

Sware
Founded: 2015
United States
www.sware.com/products/res_q

Videos and Screen Captures

Res_Q Screenshot 1
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Product Details

Platforms Supported
Cloud
Training
Documentation
Live Online
Webinars
Support
Online

Res_Q Frequently Asked Questions

Q: What kinds of users and organization types does Res_Q work with?
Q: What languages does Res_Q support in their product?
Q: What other applications or services does Res_Q integrate with?
Q: Does Res_Q have an API?
Q: What type of training does Res_Q provide?

Res_Q Product Features

Res_Q Additional Categories