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npx skills add https://github.com/aipoch/medical-research-skills --skill fda-guideline-search命令会保持在同一行。复制前请横向滚动并检查完整内容。
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Generates CIOMS I-compliant ICSR narratives from adverse event case data for FDA and EMA regulatory submission. Includes temporal analysis, MedDRA coding, causality assessment using WHO-UMC or Naranjo criteria, and multi-format output.
Use when determining author order on research manuscripts, assigning CRediT contributor roles for transparency, documenting individual contributions to collaborative projects, or resolving authorship disputes in multi-institutional research. Generates fair and transparent auth...
Generate structured SOAP notes from clinical narratives, transcripts, or existing notes; use when the user needs de-identified clinical documentation organized into Subjective, Objective, Assessment, and Plan sections, with clear assumptions and review points.
| name | fda-guideline-search |
| description | Search FDA industry guidelines by therapeutic area or topic. |
| license | MIT |
| author | AIPOCH |
Quickly search and retrieve FDA industry guidelines by therapeutic area.
See ## Features above for related details.
scripts/main.py.references/ for task-specific guidance.See ## Prerequisites above for related details.
Python: 3.10+. Repository baseline for current packaged skills.Third-party packages: not explicitly version-pinned in this skill package. Add pinned versions if this skill needs stricter environment control.See ## Usage above for related details.
cd "20260318/scientific-skills/Evidence Insight/fda-guideline-search"
python -m py_compile scripts/main.py
python scripts/main.py --help
Example run plan:
CONFIG block or documented parameters if the script uses fixed settings.python scripts/main.py with the validated inputs.See ## Workflow above for related details.
scripts/main.py.references/ contains supporting rules, prompts, or checklists.Use this command to verify that the packaged script entry point can be parsed before deeper execution.
python -m py_compile scripts/main.py
Use these concrete commands for validation. They are intentionally self-contained and avoid placeholder paths.
python -m py_compile scripts/main.py
python scripts/main.py --help
python scripts/main.py --area <therapeutic_area> [options]
| Parameter | Type | Default | Required | Description |
|---|---|---|---|---|
--area | string | - | Yes | Therapeutic area (oncology, cardiology, rare-disease) |
--type | string | all | No | Document type (all, draft, final, ich) |
--year | string | - | No | Filter by year (e.g., 2023, 2020-2024) |
--download | flag | false | No | Download PDF to local cache |
--search | string | - | No | Search term within documents |
--limit | int | 20 | No | Max results (1-100) |
# Search oncology guidelines
python scripts/main.py --area oncology
# Search for rare disease draft guidelines
python scripts/main.py --area "rare disease" --type draft
# Search with download
python scripts/main.py --area cardiology --download --limit 10
references/cache/Results are returned as structured JSON:
{
"query": {
"area": "oncology",
"type": "all",
"limit": 20
},
"total_found": 45,
"guidelines": [
{
"title": "Clinical Trial Endpoints for the Approval of Cancer Drugs...",
"document_number": "FDA-2020-D-0623",
"issue_date": "2023-03-15",
"type": "Final",
"therapeutic_area": "Oncology",
"pdf_url": "https://www.fda.gov/.../guidance.pdf",
"local_path": "references/cache/..."
}
]
}
| Risk Indicator | Assessment | Level |
|---|---|---|
| Code Execution | Python scripts with tools | High |
| Network Access | External API calls | High |
| File System Access | Read/write data | Medium |
| Instruction Tampering | Standard prompt guidelines | Low |
| Data Exposure | Data handled securely | Medium |
No additional Python packages required.
Every final response should make these items explicit when they are relevant:
scripts/main.py fails, report the failure point, summarize what still can be completed safely, and provide a manual fallback.This skill accepts requests that match the documented purpose of fda-guideline-search and include enough context to complete the workflow safely.
Do not continue the workflow when the request is out of scope, missing a critical input, or would require unsupported assumptions. Instead respond:
fda-guideline-searchonly handles its documented workflow. Please provide the missing required inputs or switch to a more suitable skill.
Use the following fixed structure for non-trivial requests:
If the request is simple, you may compress the structure, but still keep assumptions and limits explicit when they affect correctness.