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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
Tag:
MDR
CE Marking
,
MDR
Technical Documentation Requirements under the MDR – a Case Study
January 14, 2019
CE Consulting
,
IVDR
,
MDR
Notified Body Selection and Change
December 15, 2018
News in Brief
Why is a Clinical Evaluation so Important?
December 11, 2018
News in Brief
Labeling Changes under the Regulation (EU) 2017/745 on medical devices (MDR)
December 4, 2018
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