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Building AI-Enabled Curation Infrastructures for Biomedical R&D: Lessons from the field

November 19, 2024
11 AM PST / 2 PM EST

The increasing volume and diversity of biomedical data generated daily from internal and external sources underscores the necessity for High-Quality data products and AI-assisted data consumption. This presentation will demonstrate a curation application that integrates large language models (LLMs) with a human-in-the-loop process to streamline the development of High-Quality data products. We will also explore how these data products facilitate the implementation of AI-driven text query systems, significantly enhancing data accessibility for researchers. This integration allows for effective navigation of complex, multimodal datasets, ultimately improving the efficiency of data consumption and supporting informed decision-making in biomedical research and development.

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Real-World Applications We’ll Cover

  • Scaling clinico-genomic data integration: Large pharmaceutical organizations working with external data providers used Polly to build interoperable clinico-genomic data products 6x faster.
    Although purchased datasets are often labeled as "clean," they still lack interoperability—Polly's pipelines bridge this gap with robust integration and harmonization.

  • Information Retrieval: Drug safety monitoring teams used Polly's Knowledge Graph powered co-scientist to conversationally retrieve the right cohorts & assess drug response—cutting discovery time by 70%.

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What You’ll Learn

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Meet the Experts of this discussion
Key Takeaways
How data providers ensure adherence to quality standards through validation and compliance.
How GUI-based workflows, CLI tools, and collaborative workspaces enable streamlined data ingestion and synchronization at scale.
Understand how automated pipelines assess conformance, plausibility, and consistency, ensuring high-quality, AI-ready data products.
Key Takeaways
Reduce operational costs by streamlining data delivery through reusable, governed products.
Accelerate diagnostic development and clinical trial execution by delivering compliant, high-quality data at scale.
Improve audit readiness and regulatory confidence through governed data products and built-in quality assurance.
Equip cross-functional teams to act on trusted data—faster, and with greater confidence.
Who Should Attend?

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