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CE Marking Medical Devices
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European Authorized Representation for Manufacturers of Medical Devices
EU Authorized Representative Responsibilities
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Home
CE Marking Medical Devices
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
Library
Overview
Download Section
Supportive Information
Link Section
FAQ Section
News
Contact
About Us
Contact Persons
Contact Details
Reviews
Partners & Associates
Tag:
Vigilance
Important Notice
MDCG Q&A document on vigilance updated
December 2, 2024
Important Notice
Efficient support for medical device manufacturers: mdi Europa and the EUDAMED database
September 22, 2024
News in Brief
European Commission guidance publication update
July 12, 2024
News in Brief
MDCG published device specific vigilance guidance
February 8, 2024
Important Notice
A closer look at MDCG 2023-3 on vigilance
August 11, 2023
News in Brief
News on guidance documents
March 3, 2023
News in Brief
New Vigilance Reporting Templates and Supplementary Guidance on Vigilance Published
August 15, 2019
