Monitor | Be Vigilant | Report
Monitor | Be Vigilant | Report

Harness AI to improve
Pharma
industry

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Observe Safety & Quality
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Strive for Best Quality Pharma AI

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Best Quality AI in Pharma

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Be Vigilant about drug risk

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Be Vigilant about Drug risks

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Enrich with automatic ICSR Reports

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Enrich with automatic ICSR Reports

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Robust Clinical Trial
Robust Clinical Trial
Real World Evidence
Real World Evidence

Our Pharma solution analyzes Real World Evidence (RWE) repetitively to find the drug risks.


Real World Data (RWD) source includes wide variety of patient data from Electronic Health Record(EHR), claims, billing and health data collected from IOT and hand held devices.


Improve Trial prospects be more robust with diverse population and less bias.

Our Pharma solution analyzes Real World Evidence (RWE) repetitively to find the drug risks.

Real World Data (RWD) source includes wide variety of patient data from Electronic Health Record(EHR), claims, billing and health data collected from IOT and hand held devices.

Improve Trial prospects be more robust with diverse population and less bias.

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Drug Risk Management
Drug Risk Management
Signal Detection
Signal Detection
Detect Patients and analyze their Reports
Aggregate Reports
Periodic Safety Update Report (PSUR) Periodic Benefit Risk Eval Report (PBRER) Development Safety Update (DSUR)
Aggregate Reports
Confirm / Refute Adverse Event
Data Mine Pharmacovigilance Database Convert ICSR Data To Structured Format Calculate Statistical & Monitor Adverse Event Threshold
Causality Assessments
Challenging Pharmacovigilance Problems Relationship of Drug Vs Adverse Event
Confirm / Refute Adverse Event
Causality Assessments
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Pharmacovigilance
Pharmacovigilance

Pharmacological Science | Drug Safety

Pharmacological Science | Drug Safety

Prevent Adverse Drug Reactions (ADR)
Drug Exposure during pregnancy, breastfeeding, Overdose & Abuse Drugs

Adverse Event Reporting
QA in Pharma - Identifiable Patient, Identifiable Reporter, Suspect Drug, Adverse Event
Adverse Event Reporting
QA in Pharma - Identifiable Patient, Identifiable Reporter, Suspect Drug, Adverse Event
Risk Management
Detect Adverse Effect Signal Detection, Risk Management Plans (RMPs)
Risk Management
Detect Adverse Effect Signal Detection, Risk Management Plans (RMPs)
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Adverse Event Reporting
Adverse Event Reporting
QA in Pharma
QA in Pharma

Individual Case Safety Report (ICSR)
Prevent Duplicate Reporting
Permit follow-up for additional info
Allow Anonymous Report
Drug with various trade names across world

Vigibase Report (ICSR Global Database from WHO)
0 M
Pharmacovigilance Global Market By 2024
0 B
Countries Reporting To Vigibase
> 0
Represent World Population By
0%
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