
Proactive pharmacovigilance with AI-powered signal detection
Enhance patient safety and regulatory compliance with advanced AI algorithms that detect safety signals across multiple data sources in real-time.
Identify safety signals weeks or months before traditional methods
Monitor safety across all available data sources
Automated reporting ensures timely regulatory submissions
Proactive identification reduces patient safety risks and liability
Traditional pharmacovigilance relies heavily on spontaneous reporting systems, which capture only a fraction of adverse events and often identify safety signals too late. Manual signal detection is resource-intensive, subjective, and prone to missing subtle patterns. Regulatory authorities increasingly expect proactive safety monitoring using diverse data sources and advanced analytics.
Our platform integrates adverse event databases, electronic health records, social media monitoring, and literature surveillance to create a comprehensive safety monitoring ecosystem. AI algorithms continuously analyze this data to detect emerging safety signals, assess causality, and prioritize investigations. Automated reporting capabilities ensure regulatory compliance while reducing manual workload.
Processes data from global adverse event databases, EHR systems, social media platforms, and medical literature. Features include NLP for unstructured data analysis, machine learning models for signal detection, and automated regulatory reporting workflows. Compliant with ICH guidelines and regulatory requirements across major markets.
Join thousands of life science professionals who trust DocNexus to accelerate their research and improve outcomes.