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What is cubeSAFETY?

cubeSAFETY is a cutting-edge pharmacovigilance solution that aids safety teams in the effective management of adverse event reporting, regulatory submissions, and case processing while ensuring compliance. It complies with ICH E2B as well as various regional reporting guidelines, enabling submissions to regulatory bodies such as the FDA, EMA, CDE, MFDS, and PMDA through specialized gateways, and it can automatically convert and format data for CIOMS and XML exports. The platform features AI-enhanced medical coding recommendations, duplication detection, the ability to import CIOMS PDF files, and dynamic dashboards for tracking submissions in real-time. Furthermore, it provides seamless integration with other CRScube modules, including cubeCDMS. Designed to improve the safety case entry process, cubeSAFETY ensures exceptional data quality through built-in validation tools and streamlines workflows to meet global regulatory standards, all while reducing manual efforts and costs. In essence, this innovative platform aspires to transform the landscape of pharmacovigilance by enhancing both efficiency and accuracy in the industry, making it a valuable asset for safety teams worldwide.

What is IQVIA Vigilance Platform?

The IQVIA Vigilance Platform serves as a comprehensive solution aimed at optimizing safety and pharmacovigilance operations, which in turn boosts speed, accuracy, and overall effectiveness. Functioning in a secure Software-as-a-Service (SaaS) framework and utilizing cutting-edge proprietary technologies, including artificial intelligence, machine learning, and natural language processing, the platform delivers critical insights that improve compliance, ensure product safety, and play a pivotal role in the product development process. It thoroughly manages all elements of pharmacovigilance, overseeing cases from the initial patient reports through to their processing and submission to regulatory bodies, thus handling a variety of case types. With an intuitive interface, the IQVIA Vigilance Platform is easily accessible to affiliates, case processing teams, and professionals engaged in signal detection. By implementing a transformative approach to pharmacovigilance, it enhances compliance, enabling organizations to focus on the swift delivery of safer and more effective pharmaceuticals and medical devices. This groundbreaking platform is designed not only to satisfy current industry demands but also to foresee and accommodate future challenges in the dynamic realm of drug safety and efficacy. In doing so, it positions companies to remain at the forefront of innovation in healthcare.

Media

Media

Integrations Supported

XML
cubeCDMS
cubeCTMS

Integrations Supported

XML
cubeCDMS
cubeCTMS

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

CRScube

Date Founded

2010

Company Location

South Korea

Company Website

www.crscube.io/solution/cubesafety

Company Facts

Organization Name

IQVIA

Company Location

United States

Company Website

www.iqvia.com/solutions/safety-regulatory-compliance/safety-and-pharmacovigilance/iqvia-vigilance-platform

Categories and Features

Categories and Features

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