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Epidemiology / Health Economics & Outcomes

Publication Ready.

Looking to tell your safety story? We work closely with epidemiology, HEOR, academics and other teams outside of pharmacovigilance to design and execute data analyses to answer research questions. With highly cited in-house analysts and scientific advisors, Advera Health is here to provide data, analytics, and software to help get to conclusions faster, pass peer review, and get published.

What's Included

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. 

Advera provides data feeds of its proprietary FDA Adverse Event Reporting System (FAERS) data and Clinical Evidence data in easy to ingest and dynamically mapped formats to power your analytics. 

Perform complex queries to generate custom case series and calculate disproportionality based on any combination of parameters and custom MedDRA Queries. Case Series Analysis currently queries on 12 million+ case reports, returning results in just a few seconds.

First of its kind safety focused clinical trial outcomes database, only available in Evidex.

  • Safety outcomes and adverse events from 17,000+ trials
  • Sourced from literature reviews and clinical trial registries such as
  • On-demand pooled meta-analysis based on user defined criteria
  • Fully linked to other databases for cross-data set comparisons

What makes our data, analytics, and software 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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