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What is Tricentis Vera?

Tricentis Vera transforms Digital Validation by not only adding electronic signatures to digital documents but also by innovating the Computer Systems Validation process, thereby removing tedious and redundant documentation practices while linking compliance to high-quality software standards. Through the implementation of triggers and controls that ensure electronic signatures meet 21 CFR Part 11 requirements within Agile software testing processes, companies can significantly accelerate their market entry with Tricentis Vera. Furthermore, Vera provides a cohesive interface across multiple tools, acting as a centralized system of record that enables real-time tracking of review and approval processes for users and teams. Once validation assets are submitted for approval or achieve the required endorsements, the records are securely locked in qTest and Jira, safeguarding them from any modifications during or after the approval process. This seamless integration not only fosters enhanced collaboration but also optimizes workflows, making certain that quality and compliance are upheld throughout the software development lifecycle. In addition, Tricentis Vera's capabilities empower organizations to streamline their validation efforts while ensuring adherence to regulatory standards.

What is Res_Q?

Res_Q is an AI-powered GxP electronic validation and compliance management platform developed by Sware for pharmaceutical, biotechnology, and other regulated life sciences organizations. The software provides a centralized cloud-based environment for managing computerized system validation activities throughout the application lifecycle. Its validation management capabilities support planning, documentation, risk assessments, test execution, approvals, change management, and ongoing compliance monitoring. Agentic AI functionality automates routine administrative tasks, tracks validation progress, and identifies activities requiring review or human judgment. Intelligent risk scoring evaluates system criticality and other relevant factors to help quality teams prioritize validation activities and allocate resources. The platform includes automated asset processing that organizes uploaded vendor documentation, validation packages, protocols, and other supporting materials into searchable records. Its video-to-script feature converts recordings of on-screen software processes into structured validation scripts to simplify test documentation. Smart dashboards and analytics provide visibility into validation workloads, operational milestones, risk levels, and compliance status across departments and facilities. Res_Q supports validation requirements associated with Good Clinical Practice, Good Laboratory Practice, Good Manufacturing Practice, and artificial intelligence systems used in regulated environments. Its AI validation capabilities include risk-based documentation, change tracking, and performance monitoring aligned with GAMP 5 guidance and applicable regulatory expectations. Through Res_Q Connect, the platform integrates with enterprise applications, quality systems, and automated testing tools using governed workflows, approval controls, and traceable audit records.

Media

Media

Integrations Supported

Jira
Tricentis Tosca
qTest

Integrations Supported

Adobe Acrobat Sign
Amazon Web Services (AWS)
Benchling
LabVantage
LabWare LIMS
MasterControl
Microsoft Dynamics 365
NetSuite
Nuvolo
Okta
OpenClinica
SAP Cloud Platform
ServiceNow
Smartsheet
TraceLink
TrackWise
Veeva CRM

API Availability

API Availability

Has API

Pricing Information

Pricing not provided

Pricing Information

Pricing not provided

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Web-Based Support

Customer Service / Support

Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training

Training Options

Documentation Hub
Webinars
Online Training

Company Facts

Organization Name

Tricentis

Date Founded

2007

Company Location

United States

Company Website

www.tricentis.com/products/digital-validation-vera/

Company Facts

Organization Name

Sware

Date Founded

2015

Company Location

United States

Company Website

www.sware.com/products/res_q

Categories and Features

Compliance

Not specified

Life Sciences

Not specified

Categories and Features

Life Sciences

Not specified

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