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fss-mini-rag-github/agent-user-testing/05-medical-research/INSTRUCTIONS.md
FSSCoding a08e2b4001 Add comprehensive agent user testing scenarios 
- Created 15 real-world test scenarios across diverse industries
- Each scenario includes autonomous instructions and results placeholders
- Industries covered: engineering, healthcare, finance, education, tech, agriculture
- Scenarios test FSS-Mini-RAG with authentic professional use cases
- Complete deployment guide and validation tools included
- Ready for agent delegation and execution

Scenarios range from mechanical engineering CAD standards to
cybersecurity compliance, ensuring broad market validation.
2025-09-07 17:20:58 +10:00

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Test Scenario 05: Medical Research - Clinical Trial Protocol Development

🏢 Industry Context: Healthcare/Medical Research

Role: Clinical Research Coordinator
Task: Research regulations and best practices for designing Phase II clinical trials

📋 Scenario Description

You're a clinical research coordinator at a pharmaceutical company developing a new diabetes medication. Your team needs to design a Phase II clinical trial protocol that meets FDA requirements and follows good clinical practice (GCP) guidelines.

🎯 Your Mission (Completely Autonomous)

Step 1: Setup FSS-Mini-RAG

  1. Read the repository README.md to understand how to install FSS-Mini-RAG
  2. Follow the installation instructions for your platform
  3. Verify the installation works by running rag-mini --help

Step 2: Gather Research Materials

Create a folder called clinical-trial-research and populate it with relevant documentation:

  • FDA clinical trial guidance documents
  • ICH Good Clinical Practice guidelines
  • IRB/Ethics committee requirements
  • Patient safety and adverse event reporting protocols
  • Statistical analysis plans for clinical trials

Sources to explore:

  • FDA.gov clinical trial guidance documents
  • International Council for Harmonisation (ICH) guidelines
  • Good Clinical Practice training materials
  • Clinical research regulatory handbooks
  • Biostatistics and clinical trial design resources

Step 3: Index and Search

  1. Use FSS-Mini-RAG to index your clinical-trial-research folder
  2. Perform searches to answer these questions:
    • "What are the FDA requirements for Phase II trial design?"
    • "How should adverse events be classified and reported?"
    • "What statistical power calculations are needed for efficacy endpoints?"
    • "What informed consent elements are required?"
    • "How should patient eligibility criteria be defined?"

Step 4: Document Your Findings

Write your findings in RESULTS.md including:

  • FDA regulatory requirements for Phase II trials
  • Patient safety monitoring and reporting procedures
  • Statistical analysis and sample size calculations
  • Informed consent and ethical considerations
  • Protocol development timeline and milestones

Step 5: Evaluation

Rate FSS-Mini-RAG's effectiveness for:

  • Finding specific information across multiple documents
  • Searching complex documentation efficiently
  • Helping with research and analysis workflows
  • Overall usefulness for healthcare/medical research industry applications

📁 Deliverables

  • clinical-trial-research/ folder with research materials
  • RESULTS.md with findings and FSS-Mini-RAG evaluation
  • Documentation of your search queries and discoveries

⏱️ Expected Duration: 2-3 hours

🎓 Learning Objectives

  • Test FSS-Mini-RAG with healthcare/medical research industry content
  • Evaluate search effectiveness with domain-specific documentation
  • Assess usefulness for professional research workflows in healthcare/medical research