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Upgrading the Tech Stack: From Manual Relays to AI-Powered Precision

What the AI Co-Scientist Paper Actually Demonstrates for Biologists and Data Scientists

February 24, 2026
9 AM PT

Operating a modern CDMO increasingly requires adopting cutting-edge data infrastructure and leveraging purpose-built models.

Operational excellence requires solving critical technical problems:

  • Modeling plant capacity for ability to deliver on upcoming RFPs
  • Identifying precise genetic targets to improve cell line productivity.
  • Ensuring gene vector purity for viral manufacturing
  • Modeling in vitro assay data to accurately predict in-vivo outcomes

These are just a few of the fundamental scientific & operational challenges that define the industry today.

The foundation of these problems is in data infrastructure - critical information currently remains trapped in fragmented spreadsheets or multi-omics datasets. At Elucidata, we’re building Data products & models directly contribute to revenue goals.

In this webinar, we showcase our agent-based workflow to enable Business development teams at CDMOs to file competitive RFPs and win more deals. Our agentic system standardizes chemical properties from unstructured inquiries and helps prepare structured RFPs.

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Meet the Expert of this discussion
Kewal Mishra
Associate Solution Architect, Elucidata
Rahul Dhull
Solutions Consultant, Elucidata

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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Join us for a behind-the-scenes look at a Multi-agent AI system that achieves:
  • 93% recall across 23 key metadata fields including tissue, disease, cell line, donor ID, and treatment.
  • Outperformance of GPT-4.1 single-pass prompting on accuracy, F1 score, and traceability.
  • Curation of 4652 samples from 78 GEO datasets in days instead of weeks.
  • 4x reduction in manual effort equivalent to replacing a 3-person expert team working for 1 month.
  • Human-level accuracy, with 100% concordance on disease and 97% on gender based on CellxGene benchmarks.
  • Traceable records with field-level evidence attribution and confidence scores.
Register for our webinar to see how the Agentic AI system fits into scalable data workflows.

What You’ll Learn

You’ll see how CDMOs are evolving from data chaos to connected intelligence:

  • How unified scientific knowledge foundations that link disparate chemical libraries, CAS registries, and internal databases into a single queryable system
  • Agentic AI agents can help automate technical analysis, recognize molecular information, validate safety and quality data, and support faster, more accurate decisions across development and manufacturing workflows.
  • Enabling real-time insights via dynamic knowledge graphs instead of static reports.
  • Implementing tracking systems where every AI-driven decision is fully documented and GxP-compliant, maintain regulatory readiness while scaling automation.

Register now
Meet the Expert of this discussion
Kewal Mishra
Associate Solution Architect, Elucidata
Rahul Dhull
Solutions Consultant, Elucidata
Meet the Expert of this discussion
Kewal Mishra
Associate Solution Architect, Elucidata
Rahul Dhull
Solutions Consultant, Elucidata
What Sets polly KG Apart
Natural language querying with reasoning on
the roadmap
Cross-species graphs built from both proprietary
and public data
Custom scoring logic and domain-specific
ontology support
Seamless integration with internal tools, platforms,
and security frameworks
Who Should Attend
Translational Scientists and Discovery Leads
Computational Biologists and Data Scientists
Platform Owners, heads of R&D IT
Innovation and AI Strategy Teams
Who Should Attend
Translational Scientists and Discovery Leads
Data Science & Informatics Teams
Computational Biologists and R&D IT Leaders
Innovation & AI Strategy Teams

Why This Matters for Biomedical Researchers

Adopting a Data-Centric and OOD-aware approach is essential for delivering real therapeutic impact.

If you’re working with complex biological data, you may be asking:

  • Can generative AI truly assist in scientific reasoning, not just data analysis?

  • What does it mean for hypothesis generation, literature review, or even designing experiments?

  • Could this accelerate—not replace—my discovery pipeline?

Whether you're skeptical, curious, or already experimenting with AI in your lab—this is a session designed to ground your understanding in evidence, not speculation.

  • Accelerated development timelines: Scientific knowledge flows from research to manufacturing, enabling faster tech transfer with fewer delays, rework, and manual handoffs.
  • De-risked operations and compliance : Connected and validated data reduces errors while real-time deviation tracking improves manufacturing reliability.
  • Enhanced collaboration and throughput : Data centric program management removes data chasing and redundancy, strengthening CDMO sponsor collaboration from development to commercialization.
  • Future-ready for advanced modalities : A modern intelligence layer supports advanced therapeutics without exponential increases in operational burden.

Traditional KG

  • Accelerated development timelines: Scientific knowledge flows from research to manufacturing, enabling faster tech transfer with fewer delays, rework, and manual handoffs.
  • De-risked operations and compliance : Connected and validated data reduces errors while real-time deviation tracking improves manufacturing reliability.
  • Enhanced collaboration and throughput : Data centric program management removes data chasing and redundancy, strengthening CDMO sponsor collaboration from development to commercialization.
  • Future-ready for advanced modalities : A modern intelligence layer supports advanced therapeutics without exponential increases in operational burden.

Polly KG

Register now
Meet the Experts of this discussion
Kewal Mishra
Associate Solution Architect, Elucidata
Rahul Dhull
Solutions Consultant, Elucidata
Harshveer Singh
Director Engineering Research & Development, Elucidata
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
Translational Scientists and Discovery Leads
Computational Biologists and Data Scientists
Platform Owners, heads of R&D IT
Innovation and AI Strategy Teams
What Sets polly KG Apart
First KG to integrate molecular data alongside patient data records
Feature distillation pipeline for high-dimensional clinical and trial data
Base KG usable immediately, with flexible schema extensions
Cross-species graphs built from proprietary, public, and clinical datasets
Who Should Attend?

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