We understand the critical role that the health authorities and pharmaceutical companies play in safeguarding public health. Discover ThinkTrends Rx, our custom-tailored AI solution that offers state of the art AI tools to automate drug safety monitoring for FDA and pharmaceutical companies
We employ state-of-the-art natural language processing techniques and Generative AI to accurately match adverse reactions described in case narratives with known adverse reactions listed in FDA labeling.
This innovative approach greatly enhances pharmacovigilance efforts by:
"The technology in ThinkTrends RX is impressive. We were able to efficiently extract and catalog useful lactation information and document clinical studies for over 2,000 drugs. This project has the potential for significant public health impact for nursing mothers and infants. Analyzing lactation information in labeling is just the tip of the iceberg"
"The lactation labeling project enabled us to rapidly obtain data for questions which we encounter frequently. For example, instead of manually reviewing labeling, we were able to gather which drugs had positive/negative human milk studies and positive/negative animal milk studies. ThinkTrends RX was able to parse and retrieve this information in just clicks."
Welcome to ThinkTrends Pharmacovigilance, where we leverage cutting-edge artificial intelligence to revolutionize patient safety and drug efficacy. With our AI-driven solutions, we are pushing the boundaries of pharmacovigilance, making healthcare safer and more effective for everyone.
Streamline your pharmacovigilance processes with our AI-driven case processing solution. We automate the task of interpreting challenging clinical narratives, extracting relevant information with high accuracy and speed. This enhances data quality and consistency, providing a robust basis for further analysis and reporting.
ThinkTrends AI offers pharmaceutical companies a comprehensive solution for navigating FDA guidelines and ensuring compliance. Alongside automated documentation management, intelligent data analysis, quality control, and regulatory reporting, ThinkTrends AI utilizes its powerful capabilities to search and cross-check legal and other queries against a vast array of guidance and regulatory documents. By harnessing AI's ability to rapidly process and analyze information, pharmaceutical companies can ensure accurate interpretation of FDA guidelines, streamline compliance efforts, and make informed decisions with confidence.
Utilize AI to catch safety issues before they escalate. Our platform analyzes data from a variety of sources, such as electronic health records, social media, and clinical trial data. It's capable of detecting subtle safety signals and patterns that might elude human analysts. By identifying potential safety issues earlier, we enable faster and more effective interventions
Stay ahead of emerging safety concerns with ThinkTrends' real-time drug safety monitoring. By analyzing data from various sources in real-time, our AI provides timely alerts, allowing stakeholders to respond quickly and effectively to any safety concerns.
Improve the efficiency and accuracy of your adverse event reporting with ThinkTrends. We automate the collection and analysis of diverse data sources, including patient reports, clinical trial data, and social media data. This AI-driven approach reduces the time and resources required for data collection and analysis, promoting faster and more precise adverse event reporting.
At ThinkTrends Pharmacovigilance, we're reimagining drug safety for the digital age. Experience the power of AI and join us in making healthcare safer and more effective for everyone
