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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
Enhance your biomedical research endeavors through the most extensive database of biomedical literature available globally. By utilizing a thorough and contemporary search process, you can access a wealth of biomedical evidence that is both comprehensive and pertinent. Streamline your systematic searches with automated query generation facilitated by user-friendly search forms. Discover critical insights into drug-disease interactions and drug-drug relationships, meticulously curated through extensive indexing efforts. The rapid evolution of biomedical research and development necessitates access to exhaustive information, allowing you to identify potential risks by evaluating all known data. Furthermore, you can monitor safety standards to ensure compliance with regulations while unveiling connections that foster innovation. Embase stands out as a distinctive medical literature database where depth of content exceeds mere quantity. With Emtree indexing of full-text resources and specialized search terminology, you are empowered to locate all significant and up-to-date information, including data that may elude other databases. Scroll down to understand the compelling reasons why regulatory bodies endorse Embase within their best practice recommendations, ensuring that your research is not only thorough but also aligned with industry standards. This commitment to excellence in biomedical literature further positions Embase as an indispensable tool for researchers and practitioners alike.
API Access
Has API
API Access
Has API
Integrations
CoVigilAI
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
Elsevier
Country
Netherlands
Website
www.embase.com/landing