Our tasks as CH-REP:
- Verification of devices – Check that declarations of conformity and TD have been drawn up and that conformity assessment procedures have been carried out (certificates)
- Registration of economic operators
- Traceability of devices
- Report serious incidents and safety corrective actions in Switzerland to Swissmedic, trend reports
- Immediate forwarding of complaints and reports about suspected incidents to the Manufacturer
- Register of complaints, non-conforming devices, recalls and withdrawals
- Cooperate with Swissmedic in all preventive or corrective actions
- Documents retention requirements
WHAT MAKE US STAND OUT FROM OTHER CH-REPs?
