When In-House Developments Fall under the CRA
“This doesn't affect us, we don't even sell the software.” Compliance managers often hear this when the Cyber Resilience Act (CRA) comes up in connection with products developed in-house. The …
“This doesn't affect us, we don't even sell the software.” Compliance managers often hear this when the Cyber Resilience Act (CRA) comes up in connection with products developed in-house. The …
On July 27, 2026, the European Commission published its guidance on applying the Cyber Resilience Act (C(2026) 5252). It is aimed at manufacturers and other economic operators who need to …
The Cyber Resilience Act (Regulation (EU) 2024/2847), or CRA, applies in full from December 11, 2027 . The budgets that cover this date fund exactly the period in which the …
Many manufacturers assume that the Cyber Resilience Act (Regulation (EU) 2024/2847), or CRA, forces them to get IEC 62443 certification. It does not. For a large share of products, the …
Manufacturers working with IEC 62443 often ask one question first: “Which security level does our product have to meet?” The short answer is that you do not decide this alone. …
Since September 11, 2026, manufacturers of products with digital elements must report actively exploited vulnerabilities and severe incidents through the central EU reporting platform. Article 14 of the Cyber Resilience …
The Cyber Resilience Act (Regulation (EU) 2024/2847), or CRA, applies directly in every EU Member State. Each Member State still decides which national authorities enforce it. This article uses Germany …
Risk assessment, risk management, threat model, threat analysis, TARA, cybersecurity risk assessment: these terms come up again and again in projects for connected products. Sometimes they mean the same thing, …
Manufacturers of machinery, plant, and devices keep asking the same question about the Cyber Resilience Act (CRA): which standard should I apply to demonstrate that I meet the requirements? The …
On December 16, 2025, the European Commission presented its simplification proposal COM(2025) 1023 for the Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). Most attention …
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