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What is Validfor?

Validfor is a powerful and secure digital validation solution that brings all aspects of the validation process into one cohesive, paperless system, designed specifically for industries with stringent regulations. This platform effectively simplifies validation responsibilities while ensuring compliance with essential standards such as GAMP 5, 21 CFR Part 11, and EU Annex 11. By supporting electronic records and sophisticated electronic signatures, Validfor delivers complete audit trails and tailored workflows for different roles, including Author, Reviewer, and Approver, all while ensuring comprehensive CSV compliance. It systematically organizes all documentation and records in a centralized repository, diligently monitoring every change to preserve data integrity and uphold Quality Assurance. Moreover, Validfor includes integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, which aid in conducting seamless impact assessments, tracking Corrective and Preventive Actions (CAPA), managing Computer Software Assurance (CSA), and overseeing audit-ready lifecycles. This all-encompassing strategy not only boosts operational efficiency but also fortifies compliance throughout a wide range of validation activities, making it an indispensable tool for regulated industries. In this way, Validfor empowers organizations to navigate complex regulatory landscapes with confidence and precision.

What is Scilife?

Revolutionize your Life Sciences operations by greatly improving the control, efficiency, and overall quality of both your products and processes. With our fully compliant platform that has undergone pre-validation according to GAMP5 standards, you can consistently maintain inspection readiness. Achieve complete oversight of your processes and documentation, enabling perfectly tailored workflows and maximizing automation wherever possible. Enjoy seamless operations and extensive traceability through our interconnected modules that work in harmony. Our dedicated team is always on hand to respond to any inquiries you may have, ensuring you have the support you need. We are committed to delivering an exceptional Scilife experience that aligns with our high standards! The Scilife platform not only simplifies but also automates and organizes every element of your industry, whether it pertains to Medical Devices, Pharma & Biotech, or ATMP. Click below to discover the specific Scilife modules designed to address the unique lifecycle stages relevant to your field. Our software is fully outfitted with all the crucial quality tools you would expect, along with a host of additional features that exceed your expectations, empowering your operations to flourish. Join us on this exciting journey of transformation, and let’s elevate your capabilities together!

Media

Media

Integrations Supported

AuthPoint
Microsoft Azure
Microsoft Excel

Integrations Supported

AuthPoint
Microsoft Azure
Microsoft Excel

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$1000
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

Validfor

Date Founded

2024

Company Location

Estonia

Company Website

validfor.com

Company Facts

Organization Name

Scilife

Date Founded

2017

Company Location

Belgium

Company Website

www.scilife.io

Categories and Features

Categories and 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

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