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Average Ratings 0 Ratings
Description
Clinevo Safety serves as a comprehensive, cloud-based pharmacovigilance and drug safety solution that is both user-friendly and compliant with regulatory standards. This all-encompassing platform incorporates various functions, including PV intake, case processing, regulatory submissions via an AS2 gateway, analytics, and safety signal detection. Leveraging a straightforward technology architecture, it allows for significant configuration options with minimal need for customizations, resulting in reduced total ownership costs and straightforward maintenance. Users benefit from alerts for cases approaching their deadlines, ensuring they remain compliant in a timely manner. The system features advanced automation and AI capabilities that enhance case processing efficiency, while its easily configurable dynamic workflows facilitate faster case management. Through sophisticated analytics, the platform provides users with impactful and actionable insights. As a web-based application, it can be accessed from any device, at any time, using common browsers such as Internet Explorer, Chrome, and Firefox, making it exceptionally convenient for users on the go. Furthermore, its design prioritizes usability, ensuring that all users can navigate the system with ease and confidence.
Description
Streamlined surveillance of diverse data sources, seamlessly integrated with a GVP IX compliant signal management platform, can revolutionize your safety data handling. The Evidex platform offers a ready-to-go, GVP-IX compliant signal management solution that simplifies your operations without the hassle of switching between various services. By modernizing your management processes, you can ensure they are audit-proof and efficient. This automation not only helps meet regulatory standards but also enhances the overall value generated for your organization. With automated signal detection, you can identify safety signals from established sources such as ICSR databases, the FDA's Adverse Event Reporting System (FAERS), VigiBase, and clinical trial data. Furthermore, you can incorporate additional data sources, including claims, electronic health records (EHR), and other unstructured information. By aggregating these diverse data pools, you can significantly improve signaling algorithms, streamline validations and assessments, and accelerate responses to pressing drug safety inquiries. Ultimately, this approach transforms how organizations manage and leverage safety data for better outcomes.
API Access
Has API
API Access
Has API
Integrations
Amazon EC2
Amazon RDS
Amazon Web Services (AWS)
Google Chrome
Internet Explorer
Microsoft Edge
Mozilla Firefox
PostgreSQL
Integrations
Amazon EC2
Amazon RDS
Amazon Web Services (AWS)
Google Chrome
Internet Explorer
Microsoft Edge
Mozilla Firefox
PostgreSQL
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
Clinevo Technologies
Founded
2016
Country
India
Website
www.clinevotech.com/products/pharmacovigilance-software-for-drug-safety
Vendor Details
Company Name
Advera Health Analytics
Founded
2010
Country
United States
Website
www.adverahealth.com