Adverse Event Monitoring

Intelligent safety monitoring across EU markets

The Rising Cost of Missed Signals

Adverse event detection in social media requires sophisticated technology that can identify potential safety signals in multiple languages and contexts.

Manual monitoring is time-consuming and error-prone, while generic tools miss critical mentions.

HOW OPTYMOUS CAN HELP

Your Intelligent Pharmacovigilance Copilot

Understands
Pharma

Purpose-built for pharma companies, our platform recognises medical terminology, drug names, and safety signals that generic social listening tools miss.

Higher signal
Accuracy

Specialized algorithms deliver 42% more accurate adverse event detection by understanding the context and severity of safety signals across social channels.

12+
Languages

Seamlessly monitor conversations across European markets with AI that understands local medical terminology and regional reporting requirements.

FAQ

Frequently Asked Questions

How does pharmacovigilance software detects adverse events across different languages?

AI-powered social listening platform use advanced natural language processing trained specifically for pharmaceutical and medical terminology in 12+ European languages.

The system automatically identifies potential safety signals across social media, forums, and healthcare platforms, with 40% higher accuracy than traditional monitoring methods.

What makes your adverse event reporting system compliant with EU regulations?

Our platform is built specifically for European pharma compliance, incorporating EMA guidelines, GDPR requirements, and local regulatory frameworks. It includes automated reporting templates, audit trails, and documentation systems that adapt to each market's specific requirements.

Can your social media monitoring tool integrate with our existing pharmacovigilance systems?

Yes, our platform seamlessly integrates with major safety databases, CRM systems, and document management tools. We provide API access and secure data transfer protocols to ensure smooth integration with your existing pharmacovigilance workflow.

How quickly can we implement your adverse event detection system?

Most mid-size pharma companies can be fully operational within 2-6 weeks. Our implementation process includes system setup, team training, custom configuration for your specific products and markets, and integration with your existing tools.

What sets your pharmaceutical social listening platform apart from general social monitoring tools?

Unlike generic social listening tools, our platform is purpose-built for pharmaceutical companies with specialized features including medical terminology mapping, automatic severity classification, EMA-compliant reporting, and multi-language adverse event detection across European markets.