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What is Validify?

A new automated tool has been launched for analyzing and validating cloud platforms that serve regulated industries. With a simple setup that takes only a few minutes to complete, users can eliminate weeks of laborious manual validation work. Validify automates the entire procedure, generating all essential documentation in a matter of minutes and thus eliminating the need for extensive scheduling and preparation. This tool not only detects changes made to your applications but also verifies them, ensuring accuracy. While vendors typically validate their standard releases, your customized solution necessitates a more specialized approach. By maintaining compliance on your platform, Validify instills confidence and enhances efficiency in upholding regulatory standards. As a result, this innovative solution allows organizations to shift their focus away from lengthy compliance tasks and concentrate more on driving innovation and growth. Ultimately, Validify empowers businesses to navigate the complex landscape of regulations with ease and agility.

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

Salesforce

Integrations Supported

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

API Availability

API Availability

Has API

Pricing Information

$600 per month

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

Not specified

Training Options

Documentation Hub
Webinars
Online Training

Company Facts

Organization Name

Validify

Date Founded

2019

Company Location

Israel

Company Website

www.validify.app

Company Facts

Organization Name

Sware

Date Founded

2015

Company Location

United States

Company Website

www.sware.com/products/res_q

Categories and Features

Security Validation

Not specified

Categories and Features

Life Sciences

Not specified

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