Support for products entering the EU and EEA, covering applicable-legislation screening, testing plans, technical documentation and EU declaration preparation. The conformity route depends on the product and the legislation that applies.
FCC rule scoping, SDoC or Certification route assessment, RF/EMC testing and labelling-document review for radiofrequency and digital devices entering the U.S. market. FCC ID equipment authorization is addressed separately.
Support for wireless devices subject to the FCC Certification procedure, including rule scoping, RF and exposure testing, application exhibits, TCB review coordination and FCC ID labelling checks.
A structured entry point for FDA-related services, separating food facility registration, food-contact compliance, cosmetics MoCRA, medical devices, laser products, FEI and NDC/drug listing.
U.S. FDA food-contact regulatory route assessment, compositional/migration testing, authorization-status review and conditions-of-use documentation for packaging, containers, cookware and food-processing contact parts.
Support for toys entering the EU market, covering toy-safety legislation assessment, applicable EN 71 testing, label and warning review, technical documentation and coordination with the CE conformity process.
REACH compliance support for substances, mixtures and articles, including applicability review, SVHC and Annex XVII restricted-substance testing, supply-chain evidence and regulatory communication support.
RoHS applicability review, homogeneous-material planning, restricted-substance testing, supply-chain evidence and technical-document support for electrical and electronic equipment entering the EU.
Hazard classification, 16-section SDS preparation, language and jurisdiction adaptation, and revision support based on product composition, hazard data and target-market rules. An SDS is not a general product certificate.
UN Manual of Tests and Criteria subsection 38.3 testing, type-variation assessment and test-summary support for lithium metal and lithium-ion cells, batteries and equipment. This service is not the same as complete transport classification.
Testing and compliance support for cookware, packaging, containers and food-processing contact parts under relevant China GB 4806, EU FCM, U.S. FDA 21 CFR or German LFGB requirements.
Testing based on cosmetic formulation, product type and destination market, including microbiological, physicochemical, restricted-substance, stability and packaging-compatibility work, with support for EU safety documentation and U.S. MoCRA preparation.
Country- and product-specific support for markets operating pre-shipment conformity programmes, including scope screening, standards review, testing and inspection evidence coordination, and CoC application support under the current destination-market rules.
Our team supports product testing and compliance projects through standards review, document coordination and traceable service workflows.
Standards-based review and documented workflows support consistent project coordination.
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We support product testing, certification coordination and compliance documentation for regulated markets.
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These examples describe common project communication needs and do not represent specific client testimonials or project outcomes.
Review product category, target market and existing documents to identify testing needs and missing information.
Check consistency across test reports, labels, manuals and product information for platform or customer review.
Map applicable standards, testing routes and documentation requirements for the intended market.
Coordinate samples, testing scope, report purpose and supporting documents across project stages.
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Provide product specifications, photos, manuals, target market and intended use. The applicable regulations and standards can then be reviewed against the product scope.
Provide product name, model, specifications, photos, manuals, target market, required service, sample status and any platform or customer requirements.
A test report records test scope and results; a certificate confirms a defined conformity or certification outcome; registration records information with a regulator or designated system where applicable.
The timeline is confirmed after the applicable requirements, test scope, sample readiness, document completeness and any certification or registration review steps are understood.