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MDR/IVDR

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Annex II (Section 4)

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Article 10.9

ISO 13485

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§4.1.3

ISO 13485

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§820.30

Example update from MDR
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UPDATES

Never miss a revision again

RA teams track hundreds of regulations, but when changes happen – whether it’s a sentence, section, or an entire annex – there’s often no alert. The Smart Compliance List tracks revisions at the clause level, flags changes in real time, and highlights what’s new – ensuring nothing gets missed and nothing slips past your next audit.

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HARMONISATION

Prove alignment. Spot deviations.

National rules often diverge from EU MDR, IVDR, FDA frameworks and cross-domain regulations. Hoodin maps every parent regulation to its local variants — clearly showing where markets align, and where deviations create additional requirements.

Example: Norway’s MDR alignment — “Some nuances” for two regulations

GAIN REAL-TIME CONTROL OVER APPLICABLE REGULATIONS

Meet the Smart Compliance List

The only system built to identify, justify and maintain your applicable regulations — per product, per market, in real time. Always traceable, always audit-supporting.

Compliance That Works for You

  • Always know what applies — tailored to your product and markets

  • Audit-supporting traceability — every source, every version, fully documented

  • Structured outputs for action — feed compliance steps directly into your technical file

  • Credibility assured — validated and official sources only

  • Reduce effort, lower risk — eliminate manual tracking and gaps before audits

Product overview of Smart Compliance List

SMART COMPLIANCE LIST

One List. Every Regulation. Audit Supporting.

The AI-supported tool for RA/QA teams to identify, justify and monitor applicable regulations across Europe and North America — delivering the documented evidence required by Annex II (Section 4), Article 10.9, ISO 13485 §4.1.3 and FDA 21 CFR 820.

No credit card required · Cancel anytime · Full access

2 min video · Quick product walkthrough

Product overview of Smart Compliance List with features updates, harmonisation and transitions

Regulations keep changing. Can your evidence keep up?

To stay compliant, you need more than identification of applicable regulations. RA/QA teams must:

  • Justify inclusions and exclusions

  • Validate conformity methods

  • Maintain structured, auditable evidence

Without this, compliance with Annex II (Section 4), Article 10.9 MDR/IVDR or FDA 21 CFR 820 cannot be demonstrated.

Hoodin gives you a system that evolves with every update — delivering traceable, audit-supporting documentation for confident compliance.

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TRANSITIONS

Stay ahead of regulatory change

Transition deadlines and proposals are tracked directly in your list, flagging outdated rules and highlighting upcoming changes — so you can prepare in advance, not scramble under audit pressure.

Example of a transition between regulations - transition status for regulations regarding Blood, Tissues and Cells
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SMART COMPLIANCE

Hoodin is designed for compliance with major international regulations and standards

Stop tracking regulations.
Start mastering them.

Finally, a regulatory tool that works as fast and as smart as you do.

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No credit card required

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14-day free trial

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Test ALL features

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