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CE Marking Medical Devices
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OEM – Private Labeling
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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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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:
No-Deal Brexit
Brexit
,
News in Brief
Consultation on amending UK medical devices regulations
December 2, 2021
Brexit
,
News in Brief
Additional MHRA guidance for medical device companies
January 17, 2021
Brexit
,
News in Brief
Latest UK MHRA updates on Northern Ireland and EU device regulation guidance
October 26, 2020
Brexit
,
News in Brief
New UKCA mark after Brexit
September 17, 2020
Brexit
,
News in Brief
Brexit and the regulatory situation for the medtech industry
February 3, 2020
Brexit
New Guidance for the UK Responsible Person Published
September 26, 2019
Brexit
United Kingdom (UK) to Request ‘UK Responsible Person’
August 19, 2019
Brexit
Details about the Regulation of Medical Devices in Case of No-Deal Brexit
February 28, 2019
Brexit
What about Brexit?
December 21, 2018