Your AI enabled Medical Literature Monitoring for Pharmacovigilance

Revolutionizing pharmacovigilance by automating and enhancing medical literature monitoring, ensuring patient safety and driving safer drug development

Enhance your Literature Monitoring with CoVigilAI, an all-encompassing platform for global and local medical literature surveillance, driven by AI.

Our AI-enabled medical literature monitoring solution employs advanced algorithms and data analytics to proactively detect & manage adverse drug events, ensuring patient safety and regulatory compliance in real-time

As demands on drug safety and pharmacovigilance experts continue to rise, they are faced with the challenge of accomplishing more with limited resources. Your pathway to success lies in the integration of automation, adoption of transformative technologies, and utilization of analytics-driven insights to enhance compliance and ensure product safety

Our groundbreaking medical literature monitoring solution seamlessly integrates human expertise with Generative AI, optimizing productivity and bolstering compliance. Engineered to expedite compliance processes while maximizing efficiency, our solution harnesses the synergy of industry experts alongside Generative AI.

Our comprehensive, Software as a Service (SaaS) solution for Medical Literature Monitoring

Streamlined tracking of scientific and medical publications across prominent global literature databases such as PubMed, Embase, and more. Customizable search strings facilitate an effortless pharmacovigilance literature monitoring journey.

Periodic surveillance of scientific and medical literature databases and publications from diverse local journals

Global Literature Monitoring

Localized Literature Surveillance

Automated ICSR Segmentation

Advanced algorithms that categorize Individual Case Safety Reports (ICSRs) into Valid, Potential, and Invalid cases

Automated Key Entity Detection

CoVigilAI efficiently recognizes crucial entities like patients, medications, adverse events, designated medical events, and beyond. This automated process drastically minimizes manual workload.

Compliant & Audit-Ready

CoVigilAI adheres to industry-leading practices and is primed to meet your regulatory requirements. The solution aligns seamlessly with FDA & GVP-VI guidelines for medical literature monitoring. Additionally, we also offer role-based user management and audit trail features to guarantee compliance with CFR-11 standards

Causality Assessment

Streamlined E2B R3 Report

Embedded QC workflow

Automated Task Assignment

Audit Trail

Dashboard & Reports

more...

Get in touch for a trial account & to learn more about features, compliance and use cases.

Multi-Language Capability

CoVigilAI enhanced to include 100+ languages beyond English

Spanish

French

German

Russian

Mandarin

Arabic

Japanese

Italian

Full-Text Processing using Generative AI

E2BR3 XML Narration

Generative AI based summary of Full-Text

Frequently asked questions

Is CoVigilAI solution validated ?

CoVigilAI is a GxP-compliant software system designed to meet the stringent requirements of FDA's 21 CFR Part 11 and EU Annex 11. We ensure full compliance and transparency by offering comprehensive IQ/OQ validation documentation upon system implementation.

Does CoVigilAI integrate with external systems ?

CoVigilAI’s solution architecture is crafted to seamlessly integrate with diverse systems, streamlining processes and enhancing collaboration among stakeholders across PV business functions. By automating tasks and fostering connectivity, it drives improvements in quality, compliance, and productivity.

The architecture facilitates extensive integration with external systems through RESTful APIs and file-based data exchange transactions. Our strategy for integrating with third-party solutions adheres to industry standards, leveraging web services, APIs, and open architecture principles to ensure seamless interoperability

How is the CoVigilAI solution offered ?

Our CoVigilAI solution is available through the Software as a Service (SaaS) model, featuring a standard Service Level Agreement (SLA). We also offer professional services for the seamless implementation, configuration, validation, and global deployment of CoVigilAI, including necessary system integrations.

What type of training is provided for the CoVigilAI solution ?

Our team of subject matter experts provides comprehensive CoVigilAI solution training to your designated Medical Literature screening experts using a 'Train-the-trainer' methodology.

How can I contact you ?

You can write to us at LetsAI@cognifAI.in or just fill in the form below. We are always happy to answer your questions.

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