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Regulatory assessments for your next decision
Choose the assessment that matches your question: market access, import, medical devices, release readiness, supplier evidence, digital products, materials, circularity or corporate regulatory scope.
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EU Market Access Assessment
Identify applicable EU product regulations, required compliance evidence and the next steps to bring your product to the EU market.
EU Import Compliance Assessment
Identify regulatory requirements, documentation gaps and critical steps before sourcing, shipping and importing products into the EU.
EU Medical Device & IVD Assessment
Assess EU medical device and IVD qualification, classification, conformity pathways and the evidence needed for your product.
Product Release Readiness Assessment
Determine your product's regulatory release readiness, identify missing evidence and prioritize the actions needed before market launch.
Supplier Regulatory Evidence Assessment
Evaluate supplier documentation readiness, identify missing regulatory evidence and define clear requests and corrective actions.
EU Digital Product Regulatory Assessment
Identify relevant EU cybersecurity, connected-product, data and AI requirements, including supporting evidence and next steps.
EU Chemicals & Materials Assessment
Identify applicable EU material and substance requirements, required declarations, evidence gaps and necessary verification steps.
EU Circularity & Digital Product Passport Assessment
Assess relevant EU circularity, product lifecycle and digital product passport requirements, and identify data, evidence and action needs.
Corporate Regulatory Applicability Assessment
Identify which supported EU corporate regulatory regimes may apply to your business or group, understand open questions and prioritize next steps.
Product-related initial orientation
For a concrete product-market-access question, the free EU Market Check is an optional starting point.
Open free EU Market Check →