Multi-agent orchestrator on Google ADK — clinical, supply chain, and regulatory specialists. Personal technical demo (Pfizer-themed scenario, not a client project).
This demo does not use Vertex AI Agent Engine (Google's managed ADK runtime). The ADK Web UI and orchestrator run on our own server — sufficient for a technical showcase.
Gemini inference still happens on Google's infrastructure (API callout); we do not host the model locally.
In production, Agent Engine is the stronger path: Google handles runtime security, scaling, and data-governance boundaries (VPC-SC, CMEK, audit). For this demo, self-hosted ADK + Gemini API keeps scope lean.
Click Copy, paste into the ADK chat, and watch the orchestrator route to the right specialist.
Routes to clinical_agent → query_fda_drug
What is the FDA approval status of Paxlovid? Include sponsor, approval date, and dosage form.
Give me the full FDA profile for Eliquis — indication, application number, and sponsor.
Does Xeljanz have any Black Box Warnings? What is the FDA approval status?
What is the FDA status of Comirnaty? Who is the sponsor and what is the indication?
Routes to supply_agent → query_inventory
How much aspirin inventory do we have in Newark? Is supply sufficient for the next 3 months?
What is the supply status for Eliquis at McPherson, KS? How many months of supply remain?
Show Paxlovid inventory across all Pfizer facilities. Flag any CRITICAL or LOW status.
Do we have enough Comirnaty stock at McPherson to cover Q3 demand?
Routes to regulatory_agent → query_regulation
What are the key requirements of 21 CFR Part 11 for electronic records in clinical trials?
What is the EU AI Act compliance deadline for high-risk AI systems in pharma? What are the key requirements?
Summarize ICH E6(R2) Good Clinical Practice requirements relevant to data integrity.
What does 21 CFR Part 211 require for Pfizer manufacturing sites like Newark and Kalamazoo?
Orchestrator delegates to multiple specialists
Is Paxlovid FDA approved and do we have enough inventory across all facilities for Q3?
For Eliquis: FDA approval status, current inventory at McPherson, and any relevant GMP compliance requirements.
We are planning a Phase III trial for a new compound. What GCP requirements apply, and what FDA electronic records rules must our systems meet?