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Switzerland’s Swissmedic database (swissdamed) registration deadline is approaching fast. Medical device manufacturers placing products on the Swiss market must prepare now to meet UDI device registration and economic operator requirements before July 1, 2026. In this episode of Reg with Meg, host Tiffany Brown speaks with regulatory consultant Brittany Dunning about what medical device companies must do to prepare for swissdamed compliance. They break down the practical steps companies should take now, including economic operator registration, CHRN requirements, device data preparation, and how swissdamed differs from EUDAMED. Key topics covered in this episode: swissdamed registration deadlines and timelines Economic operator registration (CHRN requirements) Device registration in the Swiss UDI Devices Module Differences between Swissdamed and EUDAMED Common compliance mistakes companies make Best practices to prepare before the July 2026 swissdamed deadline If your company manufactures, imports, or represents medical devices in Switzerland, this update is essential to avoid compliance risks and delays. Subscribe to Reg with MEG for weekly regulatory insights covering global medical device regulations, compliance updates, and industry news. #MedicalDevices #Swissmedic #RegulatoryAffairs #UDI #MedicalDeviceRegulation #Compliance