AI Compliance Documentation Generation System
Employs a 7-agent AI system that analyzes change requests, retrieves relevant regulatory knowledge via RAG, performs automated risk assessment with FMEA generation, produces GxP-compliant documents with streaming generation, validates compliance against FDA 21 CFR Part 11 and other standards, and manages human review workflows with electronic signatures..
Problem Statement
The challenge addressed
Solution Architecture
AI orchestration approach
Multi-agent orchestration interface showing 7 specialized agents collaborating on FDA 21 CFR Part 11 regulatory knowledge retrieval
Document generation package displaying 7 AI-generated compliance documents totaling 67 pages with 96% average quality score
FDA 21 CFR Part 11 compliant electronic signature workflow with multi-level approval and immutable blockchain-style audit trail
Completion summary showing 96% time reduction (60-80 hours to 2-3 hours) and 100% regulatory compliance achievement
AI Agents
Specialized autonomous agents working in coordination
Orchestrator Agent
Complex documentation workflows require coordination between analysis, knowledge retrieval, document generation, compliance validation, and human review stages.
Core Logic
The Orchestrator Agent manages the end-to-end documentation workflow. It receives change requests, creates orchestration plans, delegates tasks to specialist agents, monitors progress, handles agent collaboration and consensus building, and coordinates the human approval workflow. Tracks processing timeline and generates system metrics.
Change Analyzer Agent
Change requests arrive in various formats with inconsistent detail levels, making it difficult to systematically assess documentation requirements and risk categorization.
Core Logic
The Change Analyzer parses and normalizes change request information, identifies affected equipment and systems, determines GxP impact classification, categorizes change type (parameter modification, software update, hardware replacement), and extracts technical details for downstream processing. Generates structured change analysis output.
Regulatory Expert Agent
Compliance documentation requires accurate reference to applicable regulations, standards, and guidance documents which change frequently and are difficult to navigate.
Core Logic
The Regulatory Expert uses RAG (Retrieval Augmented Generation) to query regulatory knowledge bases including FDA guidance documents, GxP standards, ISO requirements, and IEC specifications. It identifies applicable requirements for the specific change type, retrieves relevant regulatory text, and provides citation-backed regulatory guidance to other agents.
Risk Assessor Agent
Risk assessment for manufacturing changes requires systematic analysis of patient safety, product quality, data integrity, and regulatory compliance impacts with proper severity and probability ratings.
Core Logic
The Risk Assessor performs comprehensive risk analysis including FMEA (Failure Mode and Effects Analysis) generation. It identifies potential failure modes, assesses severity/occurrence/detection ratings, calculates RPN (Risk Priority Numbers), determines risk levels (Low/Medium/High/Critical), and generates mitigation recommendations. Produces structured risk assessment outputs.
Document Generator Agent
Creating compliant documentation requires proper formatting, regulatory language, cross-references, and adherence to document control requirements which is tedious and error-prone when done manually.
Core Logic
The Document Generator produces GxP-compliant documents using approved templates with streaming generation for real-time progress visibility. It creates Impact Assessments, Risk Analysis reports, FMEA documents, Validation Protocols, and Change Control Records. Documents include proper headers, revision control, cross-references, and regulatory citations.
Compliance Validator Agent
Generated documents must be validated against multiple compliance standards to ensure they meet regulatory requirements before human review and approval.
Core Logic
The Compliance Validator performs automated compliance checking against FDA 21 CFR Part 11, GxP standards, and other applicable regulations. It validates document completeness, proper authorizations, audit trail requirements, electronic signature compliance, and data integrity controls. Generates compliance check reports with pass/fail status and remediation guidance.
Quality Reviewer Agent
Documents require quality review to ensure technical accuracy, consistency, proper formatting, and alignment with organizational standards before final approval.
Core Logic
The Quality Reviewer performs automated quality checks on generated documents including grammar and style validation, technical consistency verification, template compliance, cross-reference validation, and completeness assessment. Identifies issues requiring human attention and generates quality scorecards with improvement recommendations.
Worker Overview
Technical specifications, architecture, and interface preview
System Overview
Technical documentation
Tech Stack
7 technologies
Architecture Diagram
System flow visualization