Enhance safety and compliance with proactive adverse event monitoring. Streamline the monitoring and reporting of adverse events swiftly.
Comprehensive Events Analysis
AI-powered extraction, classification, vertical search, and analysis across domain-specific parameters, managing large volumes, multi-page reports, and diverse document types, sources, and formats.
Proactive Safety Teams
End-to-end automation eliminates repetitive, low-value tasks, offering significant time savings for Safety, Medical, Regulatory, and other related teams.
Minimise Risk, Maximize Compliance
Reduce manual errors, improve risk assessment, and automate the identification of anomalies, risk factors, regulatory requirements, and standard & non-standard event categories.
Enhanced Event Visibility
With flexible data-based triggers and alerts, you will never miss critical events or deadlines. You can also efficiently collaborate on document workflows with multiple users and roles.
Utilise AI-powered data extraction from over 100,000 reports, with classification, aggregation, and automated insights generation. Our solution ensures compliant monitoring and efficient reporting.
Leverage AI-powered extraction of thousands of data points from unstructured documents, such as PDF, XML, Excel, and so on, from multiple sources (web, cloud storage, APIs, etc.), with the flexibility to configure any relevant parameters. Handle legacy reports in bulk and automate document classification based on defined criteria and event types.
Automate alerts and trigger notifications customised to specific users based on critical dates, regulatory requirements, and event categories (standard, non-standard), ensuring your team stays prepared and can proactively handle adverse event stages and milestones. Seamless integration with downstream systems (e.g., Salesforce CRM) or repositories via webhooks, connectors, etc.
Powerful cognitive vertical search engine that queries across documents based on relevant search filters – such as drug name, adverse event type, or patient ID, etc. – to enable pharmaceutical companies to discover relevant information and documents quickly; in addition, semantic search that provides relevant results for Q&A-type queries.
Leverage advanced conversational AI capabilities for accurate responses to SME queries across multiple domains. Designed to understand context, sentiment, and intent, our AI solutions engage in meaningful dialogues with users. This technology transforms pharmacovigilance communications, enabling more efficient interactions between pharmaceutical databases, regulatory repositories, and healthcare providers. Our solution supports real-time query handling and issue resolution, facilitating smoother data collection, analysis, and reporting processes.
Personalized, interactive dashboards generate reports using dynamic graphs and charts. These reports highlight adverse events reported versus pending, along with average response times, offering productivity insights and aiding decision-making.
Workflow automation and integration (via APIs, webhooks) to downstream/upstream pharmacovigilance systems – thereby greatly reducing document or data duplication effort and back-and-forth coordination between entities or roles. Integrates research articles of PDF type for comprehensive data analysis.
PV Automation Solution that generates results from day 1
Automatically extract, normalise, and validate pharmacovigilance data from multiple, complex records in minutes.
Reduce tedious, manual tasks in pharmacovigilance management and reporting processes.
Ensure compliance with industry regulations through the solution's secure, private cloud deployment.
No-code AI with a simple, intuitive interface.
Up to 100% accuracy that improves over time with self-learning – critical for pharmacovigilance data.
Accuracy
Efficiency Gains
Reduced Time
Reporting throughput
Still have questions?
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How does Botminds AI enhance pharmacovigilance?
Botminds AI leverages AI agents to automate data extraction, classification, and analysis. This results in faster, more accurate adverse event monitoring, real-time alerts, and insightful reporting, ensuring patient safety and regulatory compliance.
Can Botminds AI integrate with our existing systems?
Botminds AI is designed to integrate with your current pharmacovigilance systems seamlessly. This integration ensures a smooth transition and enhances your existing workflows without disruption.
What types of documents can Botminds AI process for pharmacovigilance?
Botminds AI can process various documents, including adverse event reports, clinical trial data, regulatory submissions, literature sources, and more. Be it in a PDF, XML, HTML, Excel format the No-code platform handles diverse formats to ensure comprehensive data coverage.
How does the solution integrate with other enterprise systems?
Our solution offers APIs and connectors for seamless integration with existing ERP, CRM, and other enterprise systems.
How does Botminds AI support regulatory compliance in pharmacovigilance?
Botminds AI ensures compliance by automating compliance with regulatory guidelines and standards. Our platform generates accurate, timely reports that meet the requirements of regulatory bodies like the FDA and EMA.
What insights can Botminds AI provide from pharmacovigilance data?
Botminds AI offers detailed insights into adverse event trends, signal detection, and risk management. Our customizable dashboards present key metrics and analytics, helping you make informed decisions to enhance patient safety.
How scalable is Botminds AI's pharmacovigilance solution?
Botminds AI's solution is highly scalable, capable of handling increasing volumes of data and expanding to meet the growing needs of your pharmacovigilance operations. Our platform can adapt to both small-scale and large-scale implementations.
Learn how Botminds Intelligent Document Process can drive ROI, reduce costs, and save time for your business.