-Bayer’s modular, multi-agent GenAI platform for extracting insights from Real-World Data (RWD) and Real-World Evidence (RWE).
-How specialized agents handle data curation, harmonization, and evidence generation across complex healthcare datasets.
-Governance, scalability, and compliance considerations for deploying GenAI in regulated pharma environments.
-Data quality and integrity: Establish rigorous processes for data collection, review, and cleansing. High-quality data is essential for training reliable AI models.
-Data integration and management: Working with various data types, including chemical data, biological data, clinical outcomes, patient records, and realworld evidence. Integrate these data sources and establish effective data management systems and practices.
-Human-machine interaction: Preparing your organization for the integrated use of AI through data and AI competency programs, continuing education, and change management.
-Legal and ethical considerations: Understanding AI law. Ethical implications of AI, including bias in AI models and the impact of AI decisions in clinical settings.
-We have developed systems based on GenAI to rank and explain targets
-The system is based on literature, clinical trial documents, and knowledge graph
-Current state-of-the-art LLMs are able to analyze multi-modal data and provide comprehensive evaluation of the targets
-Pipeline can produce in few hours comprehensive summary of possible targets for a disease
-Important role of biobanks and recent large proteomic studies/cohorts
-AI versus standard statistical models in the context of omics data analysis
-Examples in metabolic health, cancer, brain health, and infectious diseases