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Protocol Deviation VS AI Act Gap

Compare Protocol Deviation VS AI Act Gap and see what are their differences

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Protocol Deviation logo Protocol Deviation

eClinical platform for clinical trials

AI Act Gap logo AI Act Gap

Free technical gap checker for the EU AI Act. Identifies which artifacts you're missing - not just your risk tier. No login. PDF report included.
  • Protocol Deviation Landing page
    Landing page //
    2022-11-18
  • AI Act Gap The homepage hero + comparison table
    The homepage hero + comparison table //
    2026-03-28
  • AI Act Gap The assessment in progress
    The assessment in progress //
    2026-03-28
  • AI Act Gap The assessment in progress
    The assessment in progress //
    2026-03-28
  • AI Act Gap The assessment results
    The assessment results //
    2026-03-28
  • AI Act Gap The generated PDF
    The generated PDF //
    2026-03-28

AI Act Gap is a free technical readiness checker for the EU AI Act. Unlike most free tools that only classify your risk tier, AI Act Gap identifies which specific technical pillars and artifacts you're missing - and tells you exactly what to build to close each gap.

The assessment is role-aware from step one: it branches differently for Providers and Deployers, and automatically detects Article 25 reclassification if you've modified or rebranded a third-party AI system. It covers high-risk systems under Annex III (Articles 9–17) and General-Purpose AI models under Articles 53–55.

Results include a downloadable PDF report with gap analysis, article references, enforcement deadlines, and recommended actions - plus an executive summary your board can read. Share a link to your results with teammates or legal counsel instantly. No login. No data stored. Verified against the final published text of Regulation EU 2024/1689.

Protocol Deviation features and specs

No features have been listed yet.

AI Act Gap features and specs

  • Assessment type
    Technical gap analysis per pillar
  • Output
    Downloadable PDF report
  • Role detection
    Provider vs Deployer, branched assessment
  • Article 25 check
    Automatic reclassification detection
  • Coverage
    High-risk (Annex III) + GPAI (Arts. 53–55)
  • Artifact guidance
    Annex IV checklist included
  • Gap prioritisation
    Critical / Important / Nice-to-have per gap
  • Enforcement deadlines
    Per-gap deadline shown in report
  • Sharing
    Shareable results link
  • Progress tracking
    Reassess anytime, compare over time
  • Login required
    No
  • Data storage
    Data storage

Analysis of Protocol Deviation

Overall verdict

  • Protocol Deviation appears to be a niche resource focused on clinical trial and research compliance topics, which can be valuable for those in the industry, though independent verification of its authority, accuracy, and update frequency is recommended before relying on it for critical decisions.

Why this product is good

  • Focuses on a specialized topic (protocol deviations in clinical research) that is often underserved by general resources
  • May offer practical guidance for handling deviations, documentation, and regulatory compliance
  • Can serve as a convenient reference point for clinical research professionals seeking quick information

Recommended for

  • Clinical research coordinators and associates managing trial compliance
  • Regulatory affairs and quality assurance professionals in life sciences
  • Sponsors, CROs, and site staff needing guidance on documenting and reporting protocol deviations
  • Students or newcomers learning about Good Clinical Practice (GCP) and trial management

Analysis of AI Act Gap

Overall verdict

  • AI Act Gap appears to be a useful compliance-focused tool for organizations navigating the EU AI Act, offering gap analysis capabilities that help identify where a company's AI systems and practices fall short of regulatory requirements. However, as with any specialized compliance service, its true value depends on the depth of its regulatory coverage, the accuracy of its assessments, and how well it integrates with your existing governance processes. Prospective users should verify the service directly and consider a trial or demo before committing.

Why this product is good

  • It focuses specifically on the EU AI Act, a complex and evolving regulatory framework where dedicated tooling can save significant time and reduce compliance risk.
  • Gap analysis tools can help organizations quickly identify areas of non-compliance and prioritize remediation efforts.
  • A specialized solution may offer clearer guidance than generic compliance software, translating dense legal requirements into actionable steps.
  • It can support documentation and audit-readiness, which is increasingly important as enforcement of the AI Act ramps up.

Recommended for

  • Companies developing or deploying AI systems that fall under the scope of the EU AI Act
  • Compliance and legal teams needing to assess regulatory gaps efficiently
  • Organizations preparing for AI Act audits or certification
  • Risk and governance officers seeking to systematize AI compliance
  • Businesses entering the EU market with AI-driven products or services

Protocol Deviation videos

+ Add

Protocol Deviations

More videos:

  • Review - What Is A Protocol Deviation?
  • Review - The Differences Between Protocol Deviations and Violations In Clinical Research Both Minor and Major

AI Act Gap videos

No AI Act Gap videos yet. You could help us improve this page by suggesting one.

Add video

Category Popularity

0-100% (relative to Protocol Deviation and AI Act Gap)

Protocol Deviation

AI Act Gap

Clinical Trial Management System
100 100%
Clinical Trial Management System
0% 0
Governance, Risk And Compliance
0 0%
Governance, Risk And Compliance
100% 100
Compliance
100 100%
Compliance
0% 0
Compliance Management
0 0%
Compliance Management
100% 100

Questions & Answers

As answered by people managing Protocol Deviation and AI Act Gap.

Which are the primary technologies used for building your product?

AI Act Gap's answer:

Next.js 14, TypeScript, Tailwind CSS, AWS, Plausible Analytics

What makes your product unique?

AI Act Gap's answer:

Only free tool that gives a technical gap report per pillar, not just a risk classification.

How would you describe the primary audience of your product?

AI Act Gap's answer:

Technical teams, AI Providers and Deployers preparing for EU AI Act compliance.

Why should a person choose your product over its competitors?

AI Act Gap's answer:

Most free EU AI Act tools tell you your risk tier and link you to articles. AI Act Gap tells you which technical pillars you're missing and exactly what to build to fix them. It's the only free tool with a downloadable gap report, Article 25 reclassification detection, and an Annex IV artifact checklist — no login, no email required.

What's the story behind your product?

AI Act Gap's answer:

AI Act Gap was built by a technical founder who kept seeing the same problem: teams knew they were high-risk under the EU AI Act but had no clear picture of which specific artifacts they were missing. Every free checker stopped at risk classification. AI Act Gap was built to go further — mapping obligations to concrete technical deliverables, verified against the final published text of Regulation EU 2024/1689.

User comments

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What are some alternatives?

When comparing Protocol Deviation and AI Act Gap, you can also consider the following products

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