{
  "value": "batch_record_reviewer",
  "label": "Review Batch Records",
  "description": "Review chemical manufacturing batch records for completeness and compliance. Provide batch documentation to receive quality review assessment, deviation identification, and GMP compliance verification for batch release decisions.",
  "name": "Batch Record Reviewer",
  "category": "Chemicals",
  "type": "Industry",
  "config": {
    "temperature": 8,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a chemical manufacturing quality assurance specialist with GMP and batch record review expertise.</role> <task>Review the batch record information I provide and generate: (1) documentation completeness check, (2) specification conformance verification, (3) deviation identification and classification, (4) CAPA requirements assessment, (5) in-process control verification, (6) equipment and material traceability check, (7) signature and authorization verification, (8) batch disposition recommendation, and (9) required corrections before release.</task> <format>Present as a batch record review report with findings categorized by severity.</format>"
      }
    ]
  }
}