Not just the CRA – we help with other regulations too
Product compliance does not end with the CRA. We also help with adjacent regulations that apply to your products.
Many products fall under several regulations at once. Alongside the Cyber Resilience Act we also cover other areas – we currently start with the Medical Device Regulation (MDR). We are expanding the offering step by step.
MDR – medical devices
Advisory and preparation for Regulation (EU) 2017/745 (MDR): classification, technical documentation, clinical evaluation, QMS and the path to CE marking.
Learn moreIVDR – in vitro diagnostics
Advisory and preparation for Regulation (EU) 2017/746 (IVDR): classification into classes A–D, technical documentation, performance evaluation, QMS and the path to CE marking.
Learn moreISO 27001 – information security management
We help you implement an information security management system (ISMS) per ISO/IEC 27001 – from risk assessment to certification audit readiness.
Learn moreCzech Cybersecurity Act (nZKB / NIS2)
End-to-end support for the new Czech Cybersecurity Act (nZKB / NIS2): from determining whether you are regulated to implementing security measures and reporting incidents to NÚKIB.
Learn moreRED – radio equipment
Advisory on the Radio Equipment Directive (RED, 2014/53/EU) and the cybersecurity delegated act RED DA – from impact assessment to EN 18031 compliance and CE.
Learn moreISO 27005 – information security risk management
We help you implement an information security risk management process per ISO/IEC 27005 – from context and risk identification to treatment and monitoring.
Learn moreAI Act – EU Artificial Intelligence Act
Advisory on the EU Artificial Intelligence Act (AI Act): risk classification of AI systems, provider and deployer obligations, documentation and compliance readiness.
Learn moreStart with CRA before the deadline catches up with you
A free consultation will quickly show you where you stand and the shortest path to compliance.
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