Industrial Equipment CE Compliance
Europe
We make CE compliance for industrial equipment clear and fast—so you can expand into Europe without delays
Multiple EU directives apply to industrial equipment. Don't let overlapping requirements, harmonized standards, or technical documentation slow your market entry. We coordinate your complete compliance strategy.
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Common certification pitfalls to avoid
Understand your fastest path to CE
Cost & timeline estimates
Common certification pitfalls to avoid
Supporting global consumer brands
Identify every directive that applies to your equipment
Multi-Directive Assessment & Compliance Strategy
Industrial equipment typically falls under multiple EU directives simultaneously: Low Voltage (LVD), Electromagnetic Compatibility (EMC), potentially Machinery, ATEX for explosive atmospheres, Pressure Equipment, or Radio Equipment. We map every applicable directive to your product, identify the harmonized standards that create presumption of conformity (EN 61010, EN 61326, EN 60079, etc.), and create a unified compliance strategy. You get one integrated plan instead of juggling separate consultants for each directive.
Build defensible technical documentation across all directives
Technical Documentation & Laboratory Coordination
We prepare unified technical documentation covering all applicable directives: electrical safety analysis, EMC assessment, risk evaluations, and compliance matrices. We coordinate testing with accredited labs—safety, EMC, environmental, ATEX if needed—and leverage your existing certifications (UL61010, CSA, FM, IECEx) to minimize redundant testing. Our documentation packages satisfy the most stringent market surveillance inspections while keeping testing costs 40-60% below starting from scratch.
Keep pace with evolving standards and market rules
Declaration of Conformity & Continuous Compliance Management
We issue your EU Declaration of Conformity covering all applicable directives, prepare multilingual user instructions meeting EU requirements, and register any required product databases (ATEX, medical, etc.). When harmonized standards update—EN 61010-1:2010+A1:2019 transitioning to newer editions, EMC standards evolving—we proactively assess impact and update your documentation. CE compliance becomes a managed process, not a crisis every time you modify a product or standards change.
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