GRC Artifact Index
Find the right page for your regulation, framework, or control program. Filter by topic, search by keyword, and open the artifact that matches your scope.
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AI Act Timeline and Compliance Guide
Classify AI systems and GPAI models by role, risk tier, obligation set, staged application date, and required evidence.

Cyber Resilience Act Timeline and Compliance Guide
Check product scope, operator duties, essential requirements, vulnerability handling, Article 14 reporting, conformity assessment, and CE marking.

EU MDR Scope, Classification, Evidence, and Transition Guide
Check device qualification, operator roles, Annex VIII classification, conformity assessment, QMS and technical evidence, clinical evaluation, UDI/EUDAMED, PMS, vigilance, and legacy transition.

EU CSDDD Timeline and Implementation Guide
Apply the amended CSDDD scope and 2029 application date under Directive (EU) 2026/470, including due diligence, evidence, reporting, and national enforcement.

EU Machinery Regulation Compliance Hub
Classify machinery, related products and partly completed machinery; identify economic-operator roles; map Annex III and Annex I; select the Article 25 route; and prepare release and transition evidence.

EU PPWR Packaging Compliance Hub
Classify packaging and operator roles, then map substances, recyclability, recycled content, minimisation, reuse, labelling, conformity, EPR and transition evidence under Regulation (EU) 2025/40.

EU NIS2 Timeline and Compliance Guide
Check NIS2 applicability, governance, cybersecurity risk-management measures, significant-incident reporting, and implementation evidence.

EU eIDAS Timeline and Implementation Guide
Separate electronic identification, trust services, qualified status, trusted lists, signatures, seals, time stamps, QWACs, and EU Digital Identity Wallet roles.

EU EMC Directive Compliance Hub
Classify apparatus and fixed installations, assess emissions and immunity, document standards and testing, prepare the EU declaration and CE marking, and manage operator evidence under Directive 2014/30/EU.
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