The Pharmacovigilance accelerator automates the processing of adverse event signals through effectively logging and investigating drug safety issues by leveraging BPM and Low-code.

Create your own Pharmacovigilance solution using this accelerator.

Contact us

Accelerator Overview

When an adverse event Signal is received for a drug, a complex regulatory process is triggered to validate, prioritize and analyze the Signal and define a set of recommended actions. These actions are then tracked to closure along with related documentation and reviews.

The Pharmacovigilance accelerator uses a BPM and Low-code platform to automate this process from end-to-end. It allows you to automate your business processes, business rules, manages document handling and has a modern, mobile-enabled user experience. It also provides deep insight through the Pharmacovigilance dashboard and reports.

PV-Solution-Agnostic-v4

Key Highlights

Automated-Workflow-v2

Complete Automation

End-to-end process automation of handling adverse signals
key-highlight-Business-rules

Rule-Driven Approvals

Flexible business rules for driving key decisions

Timely Updates

Flexible notifications driven by templates
Excel-Data-Entry-v5

Configurable Workflow

Handling of documents relevant to the adverse event
key-highlight-v2.4

Detailed Reports

Audit trail reports for every advert event processing

Interactive Dashboards

Interactive dashboards and reports with drill-down capability

Request a Demo

I confirm I have read the privacy policy.*

Scroll to Top