Res_QSware
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Related Products
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About
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here.
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About
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.
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Platforms Supported
Windows
Not Supported
Mac
Not Supported
Linux
Not Supported
Cloud
Supported
On-Premises
Not Supported
iPhone
Not Supported
iPad
Not Supported
Android
Not Supported
Chromebook
Not Supported
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Platforms Supported
Windows
Not Supported
Mac
Not Supported
Linux
Not Supported
Cloud
Supported
On-Premises
Not Supported
iPhone
Not Supported
iPad
Not Supported
Android
Not Supported
Chromebook
Not Supported
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Audience
Healthcare and drug development industry
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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
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Support
Phone Support
Supported
24/7 Live Support
Not Supported
Online
Supported
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Support
Phone Support
Not Supported
24/7 Live Support
Not Supported
Online
Supported
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API
Offers API
Not Supported
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API
Offers API
Supported
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Screenshots and Videos |
Screenshots and Videos |
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Pricing
No information available.
Free Version
Not Supported
Free Trial
Not Supported
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Pricing
No information available.
Free Version
Not Supported
Free Trial
Not Supported
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Reviews/
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Reviews/
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Training
Documentation
Supported
Webinars
Not Supported
Live Online
Not Supported
In Person
Not Supported
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Training
Documentation
Supported
Webinars
Supported
Live Online
Supported
In Person
Not Supported
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Company InformationIQVIA
Founded: 1982
United States
www.iqvia.com
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Company InformationSware
Founded: 2015
United States
www.sware.com/products/res_q
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Alternatives |
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Categories |
Categories |
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Integrations
Adobe Acrobat Sign
Not Supported
Benchling
Not Supported
Box
Not Supported
Docusign
Not Supported
IQVIA RIM Smart
Supported
LabVantage
Not Supported
LabWare LIMS
Not Supported
MasterControl
Not Supported
NetSuite
Not Supported
Nuvolo
Not Supported
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Integrations
Adobe Acrobat Sign
Supported
Benchling
Supported
Box
Supported
Docusign
Supported
IQVIA RIM Smart
Not Supported
LabVantage
Supported
LabWare LIMS
Supported
MasterControl
Supported
NetSuite
Supported
Nuvolo
Supported
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