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compliance-audit

Generate advisory compliance audit evidence for regulated industry standards.

1|Updated Apr 9, 2026
Search Tags:#audit#compliance#advisory#iec-62304#iso-26262#human-signoff#regulated-industries
One-click install
npx skills add https://github.com/limit5/OmniSight-Productizer --skill compliance-audit-limit5
Or copy as Structured Prompt for Agent▼
Please help me install this Agent Skill.
Skill: compliance-audit
Source: https://github.com/limit5/OmniSight-Productizer/tree/main/configs/skills/compliance-audit
Command: npx skills add https://github.com/limit5/OmniSight-Productizer --skill compliance-audit-limit5

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

This Skill eliminates the risk of unqualified compliance claims for regulated industries by providing structured, advisory-only audit checks that mandate certified human signoff for all results, ensuring alignment with medical, automotive, industrial, and military/aerospace regulatory standards.

Core Features & Use Cases

  • 12 Specialized Auxiliary Audit Skills: Pre-built checks for standards including IEC 62304, HIPAA, ISO 13485, ISO 26262, MISRA C, AUTOSAR, IEC 61508, DO-178C, and MIL-STD-882E.
  • Advisory-Only Output Guarantee: All reports explicitly mark results as advisory, require human signoff, and never issue certified, approved, or compliant final decisions.
  • Structured Evidence Reporting: Generates consistent reports with evidence inputs, advisory claims, identified gaps, and human review notes to streamline certified reviewer workflows.
  • Use Case: A medical device development team can use the IEC 62304 traceability audit skill to verify their requirement-to-test-to-release evidence chain is complete before submitting to a regulatory auditor, with all findings clearly marked for human review.

Quick Start

Use the compliance-audit skill to run an advisory PHI data leakage scan on your latest HIPAA-regulated application logs, exports, and screenshots to identify potential exposure points before human review.

Frequently Asked Questions about compliance-audit

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I prepare for an IEC 62304 compliance audit for medical device software?▼

An IEC 62304 compliance audit checks your requirement-to-test-to-release evidence chain. This skill generates structured advisory audit evidence, identifies gaps, and mandates human signoff before regulatory submission.

Can I use automated compliance audits for ISO 26262 automotive software certification?▼

Automated compliance audits for ISO 26262 provide advisory-only gap identification rather than certification. This skill generates structured evidence reports to support certified reviewer decision-making, explicitly requiring mandatory human signoff.

What is advisory-only reporting in regulated industry compliance audits?▼

Advisory-only reporting in compliance audits ensures results never issue certified or approved decisions. It generates structured evidence reports with identified gaps and mandatory human review notes to streamline certified reviewer workflows.

Does this compliance audit tool support HIPAA data leakage scanning?▼

Yes, HIPAA data leakage scanning is supported for regulated application logs, exports, and screenshots. The audit identifies potential PHI exposure points and generates advisory evidence for mandatory human review.

Why do compliance audit results require mandatory human signoff?▼

Mandatory human signoff is required to eliminate the risk of unqualified compliance claims. All advisory audit results must be reviewed by a certified reviewer to ensure alignment with medical, automotive, and industrial regulatory standards.

What standards are covered by automated compliance audit tools for regulated industries?▼

Automated compliance audit tools cover standards including IEC 62304, ISO 13485, HIPAA, ISO 26262, MISRA C, AUTOSAR, IEC 61508, DO-178C, and MIL-STD-882E across medical, automotive, industrial, and military domains.

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