FSSCoding
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- 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.
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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
- Read the repository README.md to understand how to install FSS-Mini-RAG
- Follow the installation instructions for your platform
- 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
- Use FSS-Mini-RAG to index your
clinical-trial-researchfolder - 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 materialsRESULTS.mdwith 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