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CE Marking Medical Devices
CE Marking
CE Approval
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Certificates of Free Sale
OEM – Private Labeling
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CE Consulting Electrical Equipment – EMC / LVD
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European Authorized Representation for Manufacturers of Medical Devices
EU Authorized Representative Responsibilities
EU Authorized Representative vs. Distributor
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UK Responsible Person (UKRP)
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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
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Certificates of Free Sale
FAQ
Stop your Confusion about CE Marking – read our FAQ
July 17, 2023
MDR
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News in Brief
CAMD working group publishes Q&A document regarding FSCs
July 11, 2022
