Obligations for authorised representatives, importers and distributors
The Medical Devices Ordinance (MedDO; SR 812.213) sets out requirements and responsibilities for operators in the medical devices supply chain. The following information sheet outlines the roles and obligations of the Swiss authorised representative, the importer and the distributor. Link to document Document published by Swissmedic: 10 October 2021 Subscribe to EUMEDIQ’s newsletter – Link
Obligations for authorised representatives, importers and distributors Read More »