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Safety Intelligence Engine

Screen Safety Signals at Intake, Instantly

Unify Medical Information response and Drug Safety triage. Screen every conversation for potential adverse events in real time — capturing signals manual triage leaves behind.

MedDRA Mapping Active 21 CFR Part 11 Compliant Expert Safety Oversight
RxGenius.ai - Safety Screening Workspace
Live Ingestion Stream
HCP Live Chat
"HCP reporting patient case. After taking 5mg dose of RxProduct, patient developed severe headaches and reported feeling extremely dizzy when standing up."
AI MedDRA Term Extraction
Headache (PT) System Organ Class: Nervous system disorders
High Severity
Dizziness postural (PT) System Organ Class: Nervous system disorders
Moderate
4 Elements of a Valid Case Identified
The Compliance Risk

Safety signals hidden inside routine operations

HCPs and patients often report potential side effects casually in the middle of routine medical information calls. Because MI operators are focused on answering technical questions, these safety details are often undocumented or discoverable only days later during manual review cycles.

The Solution

Immediate Point-of-Intake Screening

RxGenius.ai operates in parallel with your medical information workspace. The moment an inquiry is processed, the screening engine parses the text, checks keywords against clinical dictionaries, and highlights potential safety cases immediately, reducing reporting times from weeks to seconds.

Time to Signal Identification

Traditional Manual Triage 15+ Days Avg
Day 0 (Inquiry) Day 7 (Triage) Day 15+ (Safety Review)
RxGenius.ai AI Screening Real-Time
Day 0 (Inquiry) Intake Parser (Immediate) Safety Portal (Within Minutes)
Drug safety monitoring dashboard in a premium pharmaceutical compliance center

Pharmacovigilance Intelligence

Real-Time Safety Signal Detection

Every conversation screened, every signal logged — at the moment of intake, not weeks later.

Capabilities

Regulated Drug Safety Intelligence

Equip your Pharmacovigilance team with point-of-intake detection tools, structured mapping, and audit trails.

Point-of-Intake Detection

Scan incoming text transcripts, CRM case files, and emails automatically to detect safety signals the moment they appear.

MedDRA Classification

Automatically map raw medical expressions and symptoms directly to standard System Organ Classes and Preferred Terms.

Real-Time Surveillance

Continuous monitoring across all medical inquiry portals, replacing periodic batch files with immediate safety screening.

Human-in-the-Loop Review

Provides your safety specialists with a validation panel to review, edit, confirm, or dismiss AI-flagged signals.

Regulatory Export Support

Export safety cases as E2B(R3) XML files or structured database records, ready for ingest into Argus, ArisG, or safety vaults.

Unified Triage Data Stream

Integrate Medical Affairs and Drug Safety workspaces under a single intelligence layer, preventing data siloing.

Review Console

Safety Specialist Validation Workspace

A structured validation workspace provides safety teams with full control over case extraction details.

Safety Review Portal
Awaiting Validation
Original Interaction Excerpt

"The patient took the 5mg tablets of RxProduct once daily for 3 days. On the fourth morning, she experienced severe postural dizziness and fell. Her caregiver called us immediately."

Extracted Safety Form
Workflow

The Adverse Event Triage Pipeline

Five critical phases coordinate text ingestion, dictionary matching, specialist sign-off, and reporting.

1

Intake Stream

Inquiries are processed via portal logs, CRM records, or phone transcripts.

2

AI Parser

Sentences are scanned for keywords using natural language understanding.

3

MedDRA Map

Flagged terms are matched to standard MedDRA codes and categories.

4

Safety Audit

Safety specialists review, verify reporter details, and sign off.

5

Database Sync

Submit compliant cases directly to Oracle Argus or safety vaults.

Ready to close the gap between Medical Information and Drug Safety?

See how RxGenius.ai helps Medical Affairs and Pharmacovigilance teams catch more, work faster, and stay audit-ready — without adding headcount.

Book a Demo
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