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.