Artos at BioTechX USA 2025

We’re excited to join the life sciences community at BioTechX USA. Artos is the enterprise-grade AI platform for biopharma document authoring—trusted by leading companies across clinical, non-clinical, CMC, and safety.

Our focus this year: why getting the workflow right is critical for adoption—and how a modular architecture gives enterprises the control they need to make AI truly fit into their processes.

Getting the Workflow Right: Why Modularity Matters

AI adoption in pharma doesn’t fail because of the lack of technology that works — it fails when the software doesn't fit the workflows for the end users.

With Artos, modularity means:

• The platform adapts to your document authoring workflows instead of forcing massive change change in process.

• Enterprises can scale adoption incrementally, without spending months trying to change processes.

• Teams gain visibility, trust, and control over every step of the authoring pipeline.

What Modularity Looks Like in Artos

• Bring your own templates: Ensure every draft matches company voice and standards.

• IT teams can build their own agents: Plug in your own QC agents or add style guide agents to check for terminology and data consistency before finalizing a draft.

• Audit & governance baked in: Role-based controls and full traceability keep compliance teams confident.

• Integrations that meet you where you work: Veeva, SharePoint, Box, Google Drive, and more.

Why Workflow-First Design Wins

• Clinical Regulatory & Medical Writing: Faster reviews with reduced rework. Finalize CSRs within days of database lock.

• CMC & Non-Clinical: Defensible traceability with automated QC to verify every data point before it is inserted. Robust data engineering that works with source data in all formats.

• IT & Compliance: Secure, private cloud deployments with easy governance.

See it in Action at BioTechX

We’ll be demoing:

• A full modular workflow—Template → Add Source Data → Generate Draft → QC → Regenerate with AI → Finalize Draft → Update Source Data

• Source traceability and audit trails live in action.

• Style guide enforcement so every draft reflects your internal standards.

Let’s Connect in Philadelphia

📍 Find us at Booth #S9
📅 Pre-book a meeting