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Home
CE Marking
CE Marking
CE Approval
MDR
IVDR
Certificates of Free Sale
OEM – Private Labeling
Technical File Compilation
Declaration of Conformity
CE Consulting Electrical Equipment – EMC / LVD
CE Consulting Environmental Requirements – WEEE / RoHS
EU Authorized Representative
European Authorized Representation for Manufacturers of Medical Devices
EU Authorized Representative Responsibilities
EU Authorized Representative vs. Distributor
UK & Swiss Services
UK Responsible Person (UKRP)
Swiss Authorized Representative
EU Importer
Library
Overview
Download Section
Supportive Information
Link Section
FAQ Section
News
Contact
About Us
Contact Persons
Contact Details
Reviews
Partners & Associates
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Swiss Authorized Representative
News in Brief
Swissmedic confirms swissdamed registration fees
June 3, 2026
News in Brief
Switzerland–EU MRA: Momentum returns, but a long way to go
May 3, 2026
Important Notice
Updates for Switzerland – eIFU and device registration
August 31, 2025
Important Notice
New MIR Form 7.3.1 Now Accepted in Switzerland
June 2, 2025
News in Brief
Swissmedic launches a initiative on post-market surveillance
February 1, 2025
News in Brief
Switzerland moves closer to regulatory progress in medical technology
February 1, 2025
Important Notice
mdi Europa expands services
January 22, 2025
News in Brief
Availability swissdamed and new negotiations between the EU and Switzerland
April 5, 2024
CE Marking
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Important Notice
The UK and Switzerland need special attention
June 8, 2023
News in Brief
Swiss Federal Council to mirror extended transition timelines for MDR legacy devices
June 2, 2023
News in Brief
Swiss Medical Device Manufacturers Under Pressure
April 26, 2019
