Streamlined Document Authoring
Streamline the creation of complex clinical trial documents accelerating time-to-market
Publisher
EPAM Systems
Industry Type
Healthcare & Life Sciences
Product Details
This agent automates and streamlines the authoring of clinical trial protocols. A central SDA Agent takes user requests, interprets intent, and delegates tasks to a team of specialized agents that collaborate to complete the work.
A Workflow Agent creates and edits workflows, a Template Agent manages templates in Google Docs, a Document Agent augments content in Google Docs, an Analytical Agent provides insights from BigQuery, and a Communication Agent sends notifications through Gmail. The agents communicate using the Google Agent-to-Agent (A2A) protocol. It is designed for clinical operations, drug development, and regulatory document authoring teams in healthcare and life sciences. The solution accelerates time-to-market for therapies, reduces clinical trial costs, removes redundancies, and supports smarter, data-driven protocol design that can improve clinical success rates.
Key Use Cases
Multi-Agent Clinical Protocol Drafting
Orchestrates specialized document, template, and analytics agents over Google Agent-to-Agent protocol to author clinical study protocols in Google Docs rapidly.
Data-Driven Regulatory Compliance Authoring
Incorporates BigQuery historical trial analytics into live regulatory documents to reduce drafting redundancies and accelerate IND application submission timelines.
Explore detailed deployment path
Requires Gemini. Access integration prerequisites, specialized agent configuration guides, and implementation documentation.