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.
66 lines
3.0 KiB
Markdown
66 lines
3.0 KiB
Markdown
# Test Scenario 05: Medical Research - Clinical Trial Protocol Development
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## 🏢 **Industry Context**: Healthcare/Medical Research
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**Role**: Clinical Research Coordinator
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**Task**: Research regulations and best practices for designing Phase II clinical trials
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## 📋 **Scenario Description**
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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.
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## 🎯 **Your Mission (Completely Autonomous)**
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### **Step 1: Setup FSS-Mini-RAG**
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1. Read the repository README.md to understand how to install FSS-Mini-RAG
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2. Follow the installation instructions for your platform
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3. Verify the installation works by running `rag-mini --help`
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### **Step 2: Gather Research Materials**
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Create a folder called `clinical-trial-research` and populate it with relevant documentation:
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- FDA clinical trial guidance documents
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- ICH Good Clinical Practice guidelines
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- IRB/Ethics committee requirements
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- Patient safety and adverse event reporting protocols
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- Statistical analysis plans for clinical trials
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**Sources to explore**:
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- FDA.gov clinical trial guidance documents
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- International Council for Harmonisation (ICH) guidelines
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- Good Clinical Practice training materials
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- Clinical research regulatory handbooks
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- Biostatistics and clinical trial design resources
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### **Step 3: Index and Search**
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1. Use FSS-Mini-RAG to index your `clinical-trial-research` folder
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2. Perform searches to answer these questions:
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- "What are the FDA requirements for Phase II trial design?"
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- "How should adverse events be classified and reported?"
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- "What statistical power calculations are needed for efficacy endpoints?"
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- "What informed consent elements are required?"
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- "How should patient eligibility criteria be defined?"
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### **Step 4: Document Your Findings**
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Write your findings in `RESULTS.md` including:
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- FDA regulatory requirements for Phase II trials
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- Patient safety monitoring and reporting procedures
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- Statistical analysis and sample size calculations
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- Informed consent and ethical considerations
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- Protocol development timeline and milestones
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### **Step 5: Evaluation**
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Rate FSS-Mini-RAG's effectiveness for:
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- Finding specific information across multiple documents
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- Searching complex documentation efficiently
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- Helping with research and analysis workflows
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- Overall usefulness for healthcare/medical research industry applications
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## 📁 **Deliverables**
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- `clinical-trial-research/` folder with research materials
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- `RESULTS.md` with findings and FSS-Mini-RAG evaluation
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- Documentation of your search queries and discoveries
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## ⏱️ **Expected Duration**: 2-3 hours
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## 🎓 **Learning Objectives**
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- Test FSS-Mini-RAG with healthcare/medical research industry content
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- Evaluate search effectiveness with domain-specific documentation
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- Assess usefulness for professional research workflows in healthcare/medical research |