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Para importadores y fabricantes de productos sanitarios, cosméticos y complementos alimenticios.
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Importer of medical devices under the MDR: your obligations before you place a device on the market
Under Article 13 of the MDR, the importer of a medical device is an economic operator with its own legal duties before the device reaches the EU market. Here is the verification checklist that keeps you compliant.
Importer of medical devices under the MDR: your obligations before you place a device on the market
Importing tableware and food packaging from Asia: EU compliance for importers
Selling organic food in the EU: certification under Regulation 2018/848
PPWR: what the EU Packaging Regulation 2025/40 actually requires in 2026
Why FDA, LFGB and Chinese GB tests are not valid for EU food contact compliance
Selling food supplements in the EU: a compliance guide
