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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 DrugCard?

DrugCard is an AI-powered pharmacovigilance platform designed to help pharmaceutical companies, CROs, and drug safety teams automate routine safety intelligence workflows, reduce manual screening, and maintain audit-ready pharmacovigilance processes. The platform supports global and local medical literature monitoring, regulatory intelligence, and adverse event data management in one connected workflow. DrugCard helps PV teams detect relevant safety information faster, review AI-generated article summaries, prioritize safety-relevant publications, translate local sources, create cases from literature, and maintain full traceability across screening and review activities. DrugCard’s literature monitoring solution covers 121+ countries, 2,200+ local medical sources, and 100+ languages, combining global sources such as PubMed with local, non-indexed journals that are often difficult to monitor manually. The system provides configurable projects, automated monitoring, keyword highlighting, AI pre-assessment of safety relevance, automated reports, notifications, QC workflows, audit trails, and documentation-ready outputs. In addition to literature monitoring, DrugCard includes AI-powered Regulatory Intelligence for tracking updates from health authorities and an Adverse Event Database for centralized safety data collection, E2B(R2/R3) support, reporting, analytics, and compliant case management. DrugCard is built for pharmacovigilance teams that need scalable, transparent, and compliant automation while keeping human experts in control of final medical and regulatory decisions.

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

individual
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

DrugCard

Date Founded

2021

Company Location

Estonia

Company Website

drug-card.io

Categories and Features

Categories and Features

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