irb-application-assistant（IRB 申请助理）

IRB Application Assistant

Helps researchers prepare, review, and submit Institutional Review Board (IRB) applications. Supports drafting informed consent templates, checking protocol compliance, generating application documents, and guiding researchers through the submission workflow.

Quick Start

# Generate an informed consent template
python scripts/main.py --task consent --protocol protocol.json --output consent_form.docx

# Run a compliance check on a research protocol
python scripts/main.py --task compliance-check --protocol protocol.json --verbose

# Generate a full IRB application package
python scripts/main.py --task generate-application --config study_config.json --output irb_package/

Core Capabilities

1. Generate Informed Consent Documents

Produces compliant informed consent forms based on study parameters such as participant population, risk level, and study type.

python scripts/main.py --task consent \
  --protocol protocol.json \
  --population "adults 18+" \
  --risk-level minimal \
  --output consent_form.docx

2. Protocol Compliance Review

Checks a research protocol against IRB requirements and flags missing or non-compliant sections.

python scripts/main.py --task compliance-check \
  --protocol protocol.json \
  --ruleset federal-common-rule \
  --output compliance_report.txt

3. Application Form Generation

Generates completed IRB application forms (e.g., initial review, continuing review, amendment) from structured study data.

python scripts/main.py --task generate-application \
  --form-type initial-review \
  --config study_config.json \
  --output irb_application.docx

4. Submission Checklist Validation

Validates that all required documents and fields are present before submission.

python scripts/main.py --task validate-submission \
  --package irb_package/ \
  --output validation_report.txt

Recommended Workflow

Follow these steps for a complete IRB submission:

1. Prepare study configuration — Populate study_config.json with study title, PI details, participant population, risk level, and procedures.
2. Run compliance check — Use --task compliance-check to identify gaps in the protocol before drafting documents.

- ⛔ Checkpoint: If the compliance report flags ANY errors, resolve ALL flagged items and re-run --task compliance-check before proceeding. Do not advance to step 3 with unresolved compliance errors.

1. Generate consent document — Use --task consent to produce a compliant informed consent form tailored to the study.
2. Generate application forms — Use --task generate-application to produce the required IRB submission forms.
3. Validate submission package — Use --task validate-submission to confirm all required documents are present and fields are complete.

- ⛔ Checkpoint: If validation fails, follow this loop: review errors in validation_report.txt → fix each issue → re-run --task validate-submission → only proceed when the report shows zero blocking errors.

1. Review and submit — Manually review any remaining warnings in the compliance and validation reports before submitting to the IRB.

Quality Checklist

• [ ] Protocol includes all required sections (purpose, procedures, risks, benefits, confidentiality)
• [ ] Informed consent language is at appropriate reading level for participant population
• [ ] Risk level classification is justified and documented
• [ ] All required attachments (recruitment materials, surveys, data management plan) are included
• [ ] Compliance report reviewed and all flagged items resolved
• [ ] Submission package validated with zero blocking errors

References

• references/guide.md — Detailed documentation and field descriptions
• references/examples/ — Sample protocols, consent forms, and completed applications

Skill ID: 952 | Version: 1.0 | License: MIT