Compare signal detection data mining scores on any dataset
Small and Medium Pharma 

You Have Options.

Don't settle for expensive and clunky legacy software. You now have options. Cloud-native, software-as-a-service built with modern fully integrated pharmacovigilance workflows in mind, Evidex allows pharma companies of all sizes to take advantage of web 2.0 technology. Flexible and scalable, Evidex will grow with you as your organization grows.

What's Included

Good Pharmacovigilance Practices (GVP) facilitate the performance of pharmacovigilance and is broken out into several modules. GVP Module IX - Signal Management (GVP IX) provides general guidance and requirements on scientific and quality aspects of signal management.

We believe in creating software that people want to use and believe that you shouldn't have to be a data scientist to access and gain insight from drug safety data. 


Track signals from any data source alongside internal and external inquiries and requests. 

Seamless integration between signal detection and signal management enable tracking on any dataset. Ability to manually add signals provides for complete flexibility.

The Surveillance Module monitors safety relevant observations from various datasets including internal ICSR databases, FAERS, VigiBase, EVDAS, and more.

All standard frequentist and Bayesian disproportionality scores

What makes our signal detection solution better?

tech stack

Built on Web 2.0 technology

Evidex is cloud-native, software-as-a-service built on next generation technology with a best-in-class user interface minimizing resources needed for implementation and providing tools safety reviewers want to use.


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Best-in-class customer support

Your Evidex Product Specialist is always available to train new users, conduct refresher sessions, or answer questions on-demand. In-app chat support is available in Evidex as is an interactive, online user guide. 


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Off-the-shelf, validated data integrations

Signal detection and advanced analytics on FDA Adverse Event Reporting System (FAERS), WHO's VigiBase, and our proprietary clinical safety database are included from Day 1.  


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Ready to take the next step? 

Integrated Signal Management

Audit-proof your process by tracking safety issues from clinical trials as post-approval.

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Advanced Data Analytics

Uncover hidden patterns, unknown correlations, and trends to become a value-added partner to your organization

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