FedRAMP Authorization: What FedRAMP 20x Changed
FedRAMP authorization has changed. 20x is past the pilots and in wide-scale adoption, Key Security Indicators replaced yearly…
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CMMC Compliance: The Four-Phase Rollout Explained
CMMC compliance explained: the three levels, the four phases, and why Phase 2 on 10 November 2026 is…
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CRA Product Classification: Default, Class I, Class II, Critical
Classification decides whether you need a notified body. Article 7(1) contains the two rules that settle most cases,…
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CRA Conformity Assessment: Do You Need a Notified Body?
No harmonised standard has been cited under the CRA, so Article 32(2) currently sends every Annex III product…
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The CRA Reporting Deadline: 11 September 2026
Article 14 applies from 11 September 2026, and Article 69(3) reaches products you placed on the market years…
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EU CRA: The Cyber Resilience Act Explained
What Regulation (EU) 2024/2847 requires, the four dates that matter, and the provisions manufacturers reliably get wrong.
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VDA ISA2027: What Changed and What It Means for Your TISAX Assessment
VDA ISA2027 replaces ISA 6 for every TISAX assessment ordered from 1 January 2027. What changed in the…
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ISO 42001 vs the EU AI Act: Standard, Regulation, and How They Fit
ISO 42001 vs the EU AI Act: one is a voluntary certifiable standard, the other binding law. What…
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GDPR vs HIPAA: The Differences That Actually Matter
GDPR vs HIPAA compared: scope, who they bind, consent and lawful basis, breach deadlines and penalties — and…
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ISO 27001 vs ISO 22301: Which One Do You Actually Need?
ISO 27001 vs ISO 22301 compared: information security versus business continuity, where the two overlap, and why 27001's…
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ISO 20000 vs ITIL: The Differences That Matter
ISO 20000 vs ITIL compared: one is a certifiable standard, the other a body of practice. What each…
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ISO 20000 Internal Audit Checklist: Clause 4 to 10
A clause-by-clause ISO 20000 internal audit checklist for ISO/IEC 20000-1:2018, how to build a risk-based programme, and the…
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