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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 GoVal?

GoVal is an AI-powered validation software purpose-built to digitize the full validation lifecycle across pharma, biotech, medical device, and other life science industries. From Computer System Validation (CSV), Equipment Qualification, and various validation requirements to broader GxP compliance needs, it leverages intelligent automation to deliver streamlined digital workflows—all within a secure, paperless framework. Its customizable platform with role-based workflows enables automated reviews, approvals, and real-time visibility, backed by compliant e-signatures and audit-ready traceability. Built to meet 21 CFR Part 11, EU Annex 11, and leading GxP standards, GoVal ensures seamless regulatory alignment. Risk-based strategies at the URS level empower teams to drive targeted mitigation planning and precise test case design. GoVal AI goes further—accelerating validation timelines through generative assistance for risk assessments, documentation, and test development. An in-built Document Management System (DMS) allows users to securely store, organize, and retrieve validation documents as needed—supporting data integrity, traceability, and effortless access during audits. Integrated deviation management, change tracking, and continuously updated data simplify inspections while reducing manual errors. The result: faster deployment, lower compliance costs, and stronger ROI—delivered with clarity, control, and continuous compliance.

Media

Media

Integrations Supported

Salesforce

Integrations Supported

Salesforce

API Availability

Has API

API Availability

Has API

Pricing Information

$600 per month
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Validify

Date Founded

2019

Company Location

Israel

Company Website

www.validify.app

Company Facts

Organization Name

AdventSys Technologies

Date Founded

2015

Company Location

India

Company Website

www.govalidation.com

Categories and Features

Categories and Features

Scientific Data Management System (SDMS)

Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows

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