Simplifying Adverse Drug Reaction Reporting. The IntraVigi Reporting App is the public safety gateway into the IntraVigi pharmacovigilance ecosystem. It enables patients, healthcare professionals, and the general public to submit adverse drug reaction reports easily, securely, and confidentially.
Every report flows directly into the IntraVigi Safety Database for controlled review and regulatory processing — no double entry, no manual transfers, no data loss.
The reporting problem we solved
Under-reporting of adverse events remains one of the biggest threats to patient safety in Africa. Paper forms don't reach the regulator. Web portals don't work offline. Email is too slow and unstructured. The IntraVigi Reporting App was designed to remove these barriers while maintaining strict pharmacovigilance data integrity.
- Meets reporters where they already are — on their phone
- Works offline; syncs automatically when connection is restored
- Supports both manual structured forms and AI chatbot guidance
- Generates structured, regulator-ready data from the point of care
Key features
The IntraVigi Reporting App combines ease of use with rigorous pharmacovigilance data integrity — making reporting simple without compromising quality.
Manual ADR Reporting
Structured reporting form aligned with CIOMS and ICH requirements. Guided data capture for accuracy and completeness. Confidential and anonymous submission options. Photo attachments for medicine packaging, batch numbers, and visible reactions.
CIOMS Aligned
AI Chatbot Reporting
Conversational reporting interface for users who prefer guided interaction. Supports text and voice input. Converts unstructured narratives into structured PV data. Improves reporting quality and accessibility for users with lower health literacy.
AI-PoweredOffline-First Design
Complete a report without internet connectivity. The app syncs automatically when connection is restored. Built specifically for real African connectivity conditions — where network access is intermittent and mobile data is limited.
Works OfflineEnd-to-End Integration
All reports automatically enter the IntraVigi Safety Database data entry queue, undergo professional quality review and medical assessment, and follow the regulated PV workflow through to regulatory submission. No double entry. No data loss. No manual transfers.
Zero Manual TransferImpact & outcomes
The IntraVigi Reporting App turns every phone into a pharmacovigilance data collection point — dramatically increasing ADR reporting rates while maintaining full regulatory data quality.
Higher Reporting Rates
Removing the friction of paper forms and web portals increases ADR report volume from both patients and HCPs.
Better Data Quality
Structured forms and AI chatbot guidance produce cleaner, more complete reports than free-text email submissions.
Status Transparency
Reporters can track the status of their submission — received, under review, submitted to regulator — building trust and encouraging future reporting.
- Multi-Language Support
- Anonymous Submissions
- Real-Time Status Tracking
Who the app serves
The IntraVigi Reporting App is designed for every stakeholder who may encounter an adverse drug reaction — from patients at home to clinicians on the ward to field reps in the field.
Patients & Healthcare Professionals
Patients: if a medicine made you feel worse, your report could protect someone else — it takes less than two minutes and is completely free. HCPs: stop scribbling ADRs on paper forms. Report directly from the ward, pharmacy counter, or clinic.
Pharmaceutical Companies
Give your medical science liaisons, field reps, and customer service teams a tool that captures structured, E2B-compliant reports from the first call — feeding directly into your IntraVigi Safety Database.
Privacy & Data Protection
IntraVigi Reporting App complies with the Nigeria Data Protection Regulation (NDPR) and GDPR principles. Personal data is never sold, never shared beyond the regulated pharmacovigilance workflow, and always protected with enterprise-grade encryption.