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Description
The Drug Safety Triager, developed by Clarivate, represents an advanced pharmacovigilance tool aimed at helping life sciences organizations adhere to regulatory standards. This system, which is validated for Good Practice (GxP) compliance and prepared for audits, enhances and organizes the workflow associated with literature reviews, allowing pharmacovigilance professionals to prioritize patient safety by streamlining these processes. Fully compliant with the reporting demands of major global safety regulatory bodies, including the FDA and EMA, the Drug Safety Triager includes a comprehensive validation package with every implementation. The validation documentation is carefully constructed to meet the stringent requirements set forth by the pharmaceutical sector and health authorities. Additionally, every piece of literature referenced is subjected to a meticulous review process that ensures all user actions are recorded, creating a permanent, immutable audit trail for accountability and transparency. This innovative approach not only improves efficiency but also reinforces the commitment to maintaining high standards in patient safety and regulatory compliance.
Description
Project managers have the ability to oversee the entire systematic review journey from a unified interface, enabling them to generate tailored statistics at any moment and access project archives whenever needed, all while relying on automated task assignments, confirmations, and reminders to ensure that nothing is missed. Unlike traditional methods, SRDB introduces a novel strategy for conducting systematic reviews and analyzing data within the pharmaceutical sector, healthcare, and health economics consulting, delivering a more efficient and budget-friendly alternative regardless of the project's scale. This all-encompassing solution addresses every facet of the systematic review procedure, starting from initial searches to the final report creation, all within a singular software environment. By streamlining processes, it boosts productivity, enhances precision, and fosters increased profitability by minimizing the time required to manage and generate reliable reviews and supporting evidence, ultimately transforming the way systematic reviews are conducted. With its user-friendly design and advanced features, SRDB stands out as a game-changer in the industry.
API Access
Has API
API Access
Has API
Integrations
No details available.
Integrations
No details available.
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Clarivate
Country
United Kingdom
Website
clarivate.com/life-sciences-healthcare/research-development/pharmacovigilance-drug-safety/drug-safety-triager/
Vendor Details
Company Name
VTS Software
Country
United Kingdom
Website
www.srdb.pro
Product Features
Product Features
Task Management
Collaboration
Create Subtasks
Gamification
Gantt Charts
Mobile Access
Percent-Complete Tracking
Progress Tracking
Recurring Tasks
Reporting/Analytics
Spreadsheet View
Task Board View
Task Planning
Task Scheduling
Task Tracking
Time Tracking
To-Do List View