Transform safety data capture through a centralised solution that provides standardised data across all intake routes, increases efficiencies, and accelerates safety insights.More
Transform the capture, management & processing of adverse event, drug safety & product quality complaint data
Enable global consistency through a centralised solution for all intake sources
Streamline processes, automate transfer and reduce follow up
Accelerate analysis of individual or aggregate safety reports
Intuitive, empathy-driven interface
Simple, local language system connecting with all types of reporters supported by dynamic questioning to guide users and ensure key data is collected right first time across all intake channels.
Standardised case data
Consolidate the full process onto a single platform for all sources, with instream coding and consistency checks.
Any device, any time
Highly available cloud infrastructure with online/offline capability ensures data can be entered anywhere, at any time.
Highly configurable platform that enables deployment in line with company branding, workflows and portfolio requirements.
Seamlessly transfer data between systems to optimise the end-to-end pharmacovigilance process.
Implement a centralised solution across all intake routes to increase data visibility and drive faster signal management.
Preconfigured and verified out-of-the-box platform for rapid implementation and cost-effective deployment
Reportum® is a trusted and secure digital platform founded by a team with deep domain expertise in drug safety and software engineering
Reportum is a fully configurable drug safety reporting solution, supporting adverse events and product quality complaint intake across all channels, languages, and reporter types
Streamline safety monitoring through a simple, self-service solution
Enable patients and Healthcare Professionals to report adverse events and product quality issues directly through your website
Enable Medical Representatives to capture adverse events identified during interactions with medical staff
Ensure relevant, standardised data collection and processing through optimised intake and workflow
Ensure adverse events are captured in a consistent manner while meeting timelines for Regulatory reporting
To find out more or request a demo fill in the details below: