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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.

What is Tricentis Vera?

Tricentis Vera transforms Digital Validation by not only adding electronic signatures to digital documents but also by innovating the Computer Systems Validation process, thereby removing tedious and redundant documentation practices while linking compliance to high-quality software standards. Through the implementation of triggers and controls that ensure electronic signatures meet 21 CFR Part 11 requirements within Agile software testing processes, companies can significantly accelerate their market entry with Tricentis Vera. Furthermore, Vera provides a cohesive interface across multiple tools, acting as a centralized system of record that enables real-time tracking of review and approval processes for users and teams. Once validation assets are submitted for approval or achieve the required endorsements, the records are securely locked in qTest and Jira, safeguarding them from any modifications during or after the approval process. This seamless integration not only fosters enhanced collaboration but also optimizes workflows, making certain that quality and compliance are upheld throughout the software development lifecycle. In addition, Tricentis Vera's capabilities empower organizations to streamline their validation efforts while ensuring adherence to regulatory standards.

Media

Media

Integrations Supported

5X
Indent
Jira
Tosca
qTest

Integrations Supported

5X
Indent
Jira
Tosca
qTest

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
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

Veeva

Company Location

United States

Company Website

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

Company Facts

Organization Name

Tricentis

Date Founded

2007

Company Location

United States

Company Website

www.tricentis.com/products/digital-validation-vera/

Categories and Features

Compliance

Archiving & Retention
Artificial Intelligence (AI)
Audit Management
Compliance Tracking
Controls Testing
Environmental Compliance
FDA Compliance
HIPAA Compliance
ISO Compliance
Incident Management
OSHA Compliance
Risk Management
Sarbanes-Oxley Compliance
Surveys & Feedback
Version Control
Workflow / Process Automation

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