Use case
Drug safety is probably the most essential function within a life science company.
Early detection and risk mitigation of adverse events is critical to avoid reputational crisis, drug recalls and human losses that could severely impact a company’s earnings and income.
What do we solve?
The traditional approach of pharmacovigilance relies on human resources to process and analyze multiple sources of information; but it is costly, and severely limited in terms of volume, speed, and depth.
How do we solve it?
Our approach is to automate the extraction and integration of multiple adverse report channels, the detection and classification of potential adverse events. The analysis of relational adverse event databases to identify patterns that can mitigate risks; and the summarization of findings to support evidence based regulatory – compliance reports.
Through it, we can scale the analysis volume capacity, speed, and accuracy. Achieving not only resource savings but also efficiency, treatment safety, and quality of life for patients.
What do we deliver?
dezzai provides the client with a modular platform to increase the capability of detection and analysis of drug related adverse events:
Smart connector
Automated extraction, and integration of adverse event reports from multiple channels (email, medical reports, call center, patient support programs, etc.)
Smart validator
Classification and validation of adverse events or quality related incidents using a human trained NLP model and standard information requirements.
Smart validator
Classification and validation of adverse events or quality related incidents using a human trained NLP model and standard information requirements.
Smart database & Signal analysis
Anomaly detection, signal processing and patterns identification to determine best courses of action for risk mitigation.
Smart alerts
Automated rule-based notification system for adverse events, signals, incomplete requirements, or findings.
Smart alerts
Automated rule-based notification system for adverse events, signals, incomplete requirements, or findings.
Smart reports
Reports or summarizations of findings to support the creation of compliance reports.
Other use cases
Medical Writing AI
