Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
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.
Description
Transform your Life Sciences operations by significantly enhancing the control, efficiency, and quality of your products and processes. Maintain inspection readiness consistently with our fully compliant platform, which has undergone pre-validation in line with GAMP5 standards. Gain complete oversight of your processes and documentation, allowing for perfectly customized workflows and maximized automation wherever feasible. Experience smooth operations and comprehensive traceability through our seamlessly connected modules. Our committed team is available to address any inquiries you may have at any moment. Only the finest Scilife experience meets our high standards! The Scilife platform not only streamlines but also automates and organizes every aspect of your industry, whether in Medical Devices, Pharma & Biotech, or ATMP. Click below to explore the specific Scilife modules that cater to the distinct lifecycle stages within your industry. Our software is not just equipped with all the essential quality tools you would anticipate; it also comes with numerous additional features that surpass expectations, ensuring your operations thrive. We're excited to partner with you on this transformative journey!
API Access
Has API
API Access
Has API
Integrations
AuthPoint
Microsoft Azure
Microsoft Excel
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
$1000
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
AdventSys Technologies
Founded
2015
Country
India
Website
www.govalidation.com
Vendor Details
Company Name
Scilife
Founded
2017
Country
Belgium
Website
www.scilife.io
Product Features
Scientific Data Management System (SDMS)
Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows
Product Features
Quality Management
Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management