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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:
MDR
IVDR
,
MDR
,
News in Brief
Practical advice for setting up an MDR and IVDR compliant PMS Plan
October 22, 2020
IVDR
,
MDR
,
News in Brief
Get ready for the economic operator registration in EUDAMED
October 9, 2020
IVDR
,
MDR
,
News in Brief
EUDAMED economic operator registration module available as of December 2020
September 16, 2020
MDR
,
News in Brief
Commission to put forward another European standards request
August 24, 2020
IVDR
,
MDR
,
News in Brief
New guidance document shows how to use MDSAP audit reports for MDR/ IVDR surveillance audits
August 21, 2020
IVDR
,
MDR
,
News in Brief
Updated Q&A document on MDR and IVDR UDI requirements from the European Commission
August 12, 2020
MDR
,
News in Brief
ISO TR 20416 and PMS under the MDR
August 1, 2020
Important Notice
EU guidance on Notified Body clinical evaluation assessment reports
July 24, 2020
News in Brief
Relocation of the European Commission website on medical devices
June 30, 2020
MDR
,
News in Brief
European Commission’s device standardisation request rejected
June 23, 2020
MDR
,
News in Brief
Updated timetable for Eudamed
June 7, 2020
Important Notice
,
MDR
Clinical evaluation and equivalence – using literature under the MDR
June 5, 2020
IVDR
,
MDR
,
News in Brief
New MDR and IVDR guidance documents published by MDCG and MedTech Europe
June 1, 2020
Important Notice
,
MDR
Urgently Required MDR Guidance Documents for Clinical Evaluations and PMCF Published
April 29, 2020
Important Notice
,
MDR
MDR Postponed by One Year!
April 28, 2020
Important Notice
,
MDR
MDR Postponement – Handle with Care!
April 21, 2020
Important Notice
,
IVDR
,
MDR
MDR and IVDR guidance updates
April 9, 2020
Important Notice
,
MDR
Latest MDCG Preparedness Plan and MDR Delay
March 26, 2020
News in Brief
Usability and the MDR
March 12, 2020
News in Brief
Update on Notified Bodies
March 4, 2020
Important Notice
New guidance documents for EMDN and cybersecurity
February 13, 2020
News in Brief
Latest version of ISO 14971 on risk management and the MDR and IVDR
January 8, 2020
Important Notice
MDCG guidance documents on MDR codes and sampling of MDR and IVDR devices published
January 6, 2020
Important Notice
Guidance document for class I device manufacturers
December 23, 2019
Important Notice
,
MDR
Second MDR corrigendum published
December 18, 2019
News in Brief
Early access to Single Registration Numbers (SRN)
December 16, 2019
News in Brief
New MDR and IVDR checklists for PMS and Declaration of Conformity
December 7, 2019
News in Brief
News on symbols to be used under the MDR and IVDR
December 5, 2019
News in Brief
Technical Documentation format under the MDR and IVDR
December 1, 2019
Important Notice
,
News in Brief
News on EUDAMED
November 7, 2019
News in Brief
DARE!! Services, bsi Netherlands and bsi UK designated under the MDR and IVDR
November 6, 2019
News in Brief
Guidance on Qualification and Classification of Software under the MDR and IVDR Published
October 28, 2019
Important Notice
MDCG Guidance on MDD Certificates and SSCP under the MDR
October 15, 2019
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