Medical Device Mdr Auditor

Source: https://github.com/aipoch/medical-research-skills

Medical Device MDR Auditor

ID: 130
Version: 1.0.0
Description: Check whether medical device technical files contain required documents according to EU MDR (2017/745) regulations

When to Use

• Use this skill when the task needs Audit medical device technical files against EU MDR 2017/745 regulations.
• Use this skill for academic writing tasks that require explicit assumptions, bounded scope, and a reproducible output format.
• Use this skill when you need a documented fallback path for missing inputs, execution errors, or partial evidence.

Key Features

• Scope-focused workflow aligned to: Audit medical device technical files against EU MDR 2017/745 regulations.
• Packaged executable path(s): scripts/main.py.
• Reference material available in references/ for task-specific guidance.
• Structured execution path designed to keep outputs consistent and reviewable.

Dependencies

See ## Prerequisites above for related details.

• Python: 3.10+. Repository baseline for current packaged skills.
• dataclasses: unspecified. Declared in requirements.txt.
• enum: unspecified. Declared in requirements.txt.

Example Usage

See ## Usage above for related details.

cd "20260318/scientific-skills/Academic Writing/medical-device-mdr-auditor"
python -m py_compile scripts/main.py
python scripts/main.py --help

Example run plan:

1. Confirm the user input, output path, and any required config values.
2. Edit the in-file CONFIG block or documented parameters if the script uses fixed settings.
3. Run python scripts/main.py with the validated inputs.
4. Review the generated output and return the final artifact with any assumptions called out.

Implementation Details

See ## Workflow above for related details.

• Execution model: validate the request, choose the packaged workflow, and produce a bounded deliverable.
• Input controls: confirm the source files, scope limits, output format, and acceptance criteria before running any script.
• Primary implementation surface: scripts/main.py.
• Reference guidance: references/ contains supporting rules, prompts, or checklists.
• Parameters to clarify first: input path, output path, scope filters, thresholds, and any domain-specific constraints.
• Output discipline: keep results reproducible, identify assumptions explicitly, and avoid undocumented side effects.

Quick Check

Use this command to verify that the packaged script entry point can be parsed before deeper execution.

python -m py_compile scripts/main.py

Audit-Ready Commands

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 -h

Workflow

1. Confirm the user objective, required inputs, and non-negotiable constraints before doing detailed work.
2. Validate that the request matches the documented scope and stop early if the task would require unsupported assumptions.
3. Use the packaged script path or the documented reasoning path with only the inputs that are actually available.
4. Return a structured result that separates assumptions, deliverables, risks, and unresolved items.
5. If execution fails or inputs are incomplete, switch to the fallback path and state exactly what blocked full completion.

Overview

This Skill is used to audit the compliance of medical device technical files, checking whether documents contain necessary Clinical Evaluation Reports and Post-Market Surveillance plans according to EU MDR 2017/745 regulatory requirements.

Usage

# Check single technical file directory
python3 /Users/z04030865/.openclaw/workspace/skills/medical-device-mdr-auditor/scripts/main.py --input /path/to/technical/file --class IIa

# Batch check using JSON configuration file
python3 /Users/z04030865/.openclaw/workspace/skills/medical-device-mdr-auditor/scripts/main.py --config /path/to/config.json

# Output detailed report
python3 /Users/z04030865/.openclaw/workspace/skills/medical-device-mdr-auditor/scripts/main.py --input /path/to/technical/file --class III --verbose --output report.json

Parameters

MDR 2017/745 Check Points

1. Clinical Evaluation Report (CER)

According to MDR Annex XIV Part A, must include:

• Clinical Evaluation Plan
• Clinical Data Assessment (Literature review / Clinical investigation data)
• Clinical Evidence Analysis
• Benefit-risk Conclusion

2. Post-Market Surveillance Plan (PMS)

According to MDR Article 83 & Annex III, must include:

• PMS procedure description
• Data collection methods
• Risk assessment update mechanism
• Trend reporting mechanism

3. Post-Market Clinical Follow-up Plan (PMCF Plan)

According to MDR Annex XIV Part B, for Class IIa and above devices:

• PMCF plan document
• Clinical data continuous collection methods
• Safety and performance monitoring procedures

4. Other Key Documents

• Risk Management File (ISO 14971)
• Usability Engineering File
• Biological Evaluation Report
• Labeling & Instructions for Use

Output Format

Compliance Report Example

{
  "audit_date": "2026-02-06T06:00:00Z",
  "device_class": "IIa",
  "compliance_status": "PARTIAL",
  "findings": [
    {
      "category": "CRITICAL",
      "regulation": "MDR Annex XIV Part A",
      "item": "Clinical Evaluation Report",
      "status": "MISSING",
      "description": "Clinical evaluation report file not found"
    },
    {
      "category": "MAJOR",
      "regulation": "MDR Article 83",
      "item": "PMS Plan",
      "status": "INCOMPLETE",
      "description": "PMS plan lacks trend reporting mechanism"
    }
  ],
  "summary": {
    "total_checks": 12,
    "passed": 8,
    "warnings": 2,
    "failed": 2
  }
}

Compliance Levels