For non‑EU manufacturers, CE marking projects often require the right EU-side roles (importer/distributor, sometimes authorised person/representative) and clean documentation. We help you set up the practical path to market.
We support CE-marking related workflows across multiple product sectors (e.g., Machinery, LVD, EMC, RED, PPE, PED, ATEX). The exact pathway depends on the applicable EU act and your product.
If you’re unsure which one applies, send product details and we’ll map it.
Note: Whether an “authorised representative” is required depends on the specific EU legislation. For medical devices, the concept is explicit; for other CE marking sectors, the key is correct economic operator responsibilities and documentation.