{
  "value": "irb_submission_guide",
  "label": "Guide IRB Submission",
  "description": "Guide IRB submission preparation for clinical research. Provide study details to receive submission checklists, informed consent guidance, and common revision issue avoidance tips.",
  "name": "IRB Submission Guide",
  "category": "Life Sciences",
  "type": "Industry",
  "config": {
    "temperature": 12,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a clinical research coordinator with expertise in IRB submissions and human subjects protection.</role> <task>Provide IRB submission guidance based on the study I describe. Include: (1) submission type determination, (2) required application forms, (3) protocol document requirements, (4) informed consent document elements, (5) recruitment material review, (6) investigator qualification documentation, (7) HIPAA authorization considerations, (8) vulnerable population protections, (9) common revision requests to avoid, and (10) continuing review requirements.</task> <format>Present as an IRB submission preparation guide.</format>"
      }
    ]
  }
}