AI Gap Analysis logo
AI Gap Analysis logo
How it worksPricingSecurityPartners
  1. Home
  3. Blog

Compliance research, distilled into action.

Playbooks, implementation notes, and research for teams that need audit-ready evidence without the spreadsheet chaos.

Evidence-first updates from the team

Featured

The Ultimate ISO 13485 Audit Checklist: 8 Key Areas for 2026

Prepare for your next audit with our clause-by-clause ISO 13485 audit checklist. Covers key areas, common findings, and practical tips for success.

Feb 18, 2026iso 13485 audit checklistiso 13485medical device audit
The Ultimate ISO 13485 Audit Checklist: 8 Key Areas for 2026
What Is Regulatory Affairs? Your Complete Guide to Mastering Compliance

Feb 17, 2026

What Is Regulatory Affairs? Your Complete Guide to Mastering Compliance

Unsure what is regulatory affairs? This guide explains its role as a strategic business partner, key responsibilities, and how AI is transforming the industry.

what is regulatory affairsregulatory affairs specialistmedical device compliance
How to Conduct Internal Audits for Lasting Compliance

Feb 16, 2026

How to Conduct Internal Audits for Lasting Compliance

Learn how to conduct internal audits with our expert guide. Discover proven strategies for planning, fieldwork, and reporting to achieve real compliance.

how to conduct internal audits
  • Previous
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • Next

Ready to run your first gap?

Upload documents, import questions, and get evidence-linked answers in minutes.

Run your first gap
AI Gap Analysis logo

AI-powered gap analysis for compliance frameworks. Upload documents, get evidence-linked answers.

Follow us on LinkedIn

LinkedIn

Product

  • How It Works
  • Pricing
  • Pitch Deck
  • Security & Privacy
  • Integrations

Resources

  • Calculators
  • Blog
  • Help Center
  • Customer Stories
internal audit process
ISO compliance
Mastering Regulatory Compliance for Medical Devices

Feb 15, 2026

Mastering Regulatory Compliance for Medical Devices

Navigate regulatory compliance for medical devices with this guide. Learn to master QMS, risk management, and audit readiness in the complex global market.

regulatory compliance for medical devicesmedical device complianceISO 13485
How to Prepare for an Audit A Practical Readiness Guide

Feb 14, 2026

How to Prepare for an Audit A Practical Readiness Guide

Learn how to prepare for an audit with our practical guide. We cover everything from scoping and evidence collection to gap analysis and remediation.

how to prepare for an auditaudit readinesscompliance audit
A Practical Guide to CMMC Level 2 Compliance

Feb 13, 2026

A Practical Guide to CMMC Level 2 Compliance

Master CMMC Level 2 with our step-by-step guide. Learn the 110 controls, navigate the assessment process, and implement a roadmap to protect CUI.

cmmc level 2nist 800-171cui protection
The Ultimate ISO 9001 Internal Audit Checklist: 8 Core Areas for 2026

Feb 13, 2026

The Ultimate ISO 9001 Internal Audit Checklist: 8 Core Areas for 2026

Master your next audit with our comprehensive ISO 9001 internal audit checklist. Explore 8 key areas, sample questions, and evidence requirements for 2026.

iso 9001 internal audit checklistqms auditiso 9001 clauses
Assess Vendor Risk: A Practical Guide to (assess vendor risk)

Feb 12, 2026

Assess Vendor Risk: A Practical Guide to (assess vendor risk)

Discover how to assess vendor risk with a modern framework. This guide covers vendor tiering, evidence collection, risk scoring, and ongoing monitoring.

assess vendor riskvendor risk managementthird-party risk
Automate Regulatory Compliance: Practical Steps to Faster Audits

Feb 10, 2026

Automate Regulatory Compliance: Practical Steps to Faster Audits

Discover practical AI-driven strategies to automate regulatory compliance and pass audits faster with less stress.

automate regulatory compliancecompliance automationaudit readiness

Company

  • About
  • Contact Support
  • Partners
  • Privacy Policy

© 2026 AI Gap Analysis - Built by Tooling Studio with expert partners for human validation when needed.