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What is Visual Quality?

The categorization of all document versions or registration files into separate modules according to their status—such as draft, approved, valid, and historical—throughout their lifecycle offers a unique viewpoint on the document management framework. Creating registration forms is made easy with the built-in HTML editor, alongside customizable registration fields and workflows. Moreover, Visual Quality's registration features are notably superior to those provided by competing solutions. The management of registrations, whether they are being created or have been approved or rejected, is efficiently administered through Visual Quality Web Access. With a robust community actively participating in the evolution of the product, Visual Quality is experiencing rapid advancements. Our ambitious development timeline reflects our unwavering commitment to delivering exceptional software that helps you build and maintain your quality management system. This dedication to continuous improvement guarantees that our users will consistently benefit from the most current features and enhancements available in the market, ensuring their systems remain competitive and effective. By prioritizing user feedback and industry trends, we aim to foster a culture of innovation that drives future developments.

What is Veeva Vault RIM?

The Vault RIM Suite provides a robust platform for comprehensive management of regulatory information throughout its entire lifecycle. By consolidating global regulatory workflows within a cloud-based infrastructure, it significantly improves visibility, data integrity, and responsiveness for organizations in the life sciences sector. This centralization enables companies to quickly adjust to evolving regulations while enhancing efficiency during the submission process, from initial planning to final publication. Moreover, the platform fosters seamless collaboration among headquarters, affiliates, and partners, all integrated within a singular RIM system. It ensures that regulatory teams produce content that is trustworthy and maintains the highest standards of data quality. Veeva Vault Registrations manages product registration information globally, including registration status, variations, and interactions with health authorities, while its flexible data model is prepared to integrate IDMP data points and adapt to shifts in regulatory data standards. Additionally, Veeva Vault Submissions streamlines the submission planning process by automating numerous steps in the regulatory workflow, resulting in considerable time savings and enhanced outcomes. This comprehensive approach ultimately empowers companies to navigate the intricate landscape of regulatory compliance with increased ease and accuracy, reinforcing their capacity to succeed in a competitive environment. As regulatory landscapes continue to evolve, this platform positions organizations to stay ahead of the curve.

Media

Media

Integrations Supported

5X
Indent

Integrations Supported

5X
Indent

API Availability

Has API

API Availability

Has API

Pricing Information

$2,361
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

Visual Enterprise Solutions

Date Founded

1998

Company Location

Denmark

Company Website

www.visual-quality.com

Company Facts

Organization Name

Veeva

Company Location

United States

Company Website

www.veeva.com/products/vault-rim/

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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