Validation Automation Platform
Carefully Curated for All Validation Needs
Discover the Res_Q Platform
Through Res_Q, Sware provides one validation solution crafted for the entire life sciences industry. Res_Q automates validation – effortlessly navigating through every step of the process for GxP and non-GxP systems. Res_Q offers unparalleled value to quality, IT, and business leaders across pharmaceutical, biotech, medical device, software development, and professional services organizations.
ReportingRead More
ReadyRead More
One Central Validation Platform
Operating as a validation air traffic controller across the entire validation lifecycle - serves all areas across the enterprise (information technology, manufacturing, lab systems, and more) providing streamlined processes and centralized activities.
Intelligent Risk Assessments
Assessing risk levels based on logic programmed within and defining what the validation process is downstream, Res_Q brings forward critical thinking (what to do and not do) to put quality at the forefront while speeding up the process.
Analytics & Reporting
Delivering data for easy review and creation of informative reports to share across your organization, without the hassle of pulling information from multiple sources, Res_Q streamlines the ability to inform and make data-driven decisions across the enterprise.
Pre-built Compliance Modules
Providing a starting point from which to validate, Sware offers pre-built compliance modules for more than 30 life sciences systems. These modules provide content you can easily edit, accelerating your compliance and speeding up validation to get your team up and running quickly.
Intuitive Workflow
Starting with an easy-to-navigate process which guides you through all of the decision points and gets you to the end state of validation within the system, Res_Q ensures compliance through 100% process adherence to your validation activities.
Enterprise System Ready
Integrating with existing systems (e.g. QMS, LMS, training, and engineering) within your organization and effectively de-siloing efforts, Res_Q drives consistency and effectiveness throughout the continuum of the validation process.
Test Script Creation & Execution
Leveraging ALCOA Plus data security and integrity principles while providing access to templates for building test scripts that can be linked to documents – speeds the creation, execution, review, and approval of test scripts while ensuring data quality.
Open API
Experience the Res_Q API difference - a robust, dynamic integration that unlocks all platform functionalities. Empower developers with methodologies and use cases to harness capabilities, access data, and execute actions seamlessly. This unique integration is designed to foster innovation and supercharge efficiency, ensuring you get the most out of Res_Q's powerful features.
Featured Resources
of patients.Read More