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Need EC Rep/UKRP for both EU-27 & UK? UK & EEA (EU/EC) European Authorised Representative/Authorized Representative (UK Responsible Person) & CE Mark (CE Marking) consulting services

World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.

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Topics: brexit, ce, ce mark, ce mark (ce marking) consulting services, ec, ec rep, eu, logo, mark, marking, need ec rep/ukrp for both eu-27, symbol

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eaarmed.org

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EAAR
EAAR is the home for the professional European Authorized Representative organizations serving the Medical Device and In-Vitro Diagnostic manufacturers in accordance with the European Medical Device Directives.



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mednet-eurep.com

mednet-eurep.com mednet-eurep.com           
MEDNET - European Authorized Representative
MedNet acts as your European Authorized Representative (EC Representative) for medical devices, AIMD, IVD, cosmetic products and clinical studies.


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cmcmedicaldevices.com

cmcmedicaldevices.com cmcmedicaldevices.com           
European Authorized Representative - Consulting CE Marking - CMC Medical Devices
European Authorized Representative and Consulting CE Marking. CMC Medicaal is an official European Authorized Representative and Consulting CE Marking.


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qarad.com

qarad.com qarad.com           
home - qarad
Qarad - your regulatory gateway to Europe
Quality and Regulatory affairs, including CE marking, European Authorized Representative, Quality systems, training, translations of technical documentation, Risk management, Performance evaluations IVD, Reach/CLP



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ce-marking.net

ce-marking.net ce-marking.net           
Need EC Rep/UKRP for both EU-27 & UK? UK & EEA (EU/EC) European Authorised Representative/Authorized Representative (UK Responsible Person) & CE Mark (CE Marking) consulting services
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.


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ce-marking.eu

ce-marking.eu ce-marking.eu           
Need EC Rep/UKRP for both EU-27 & UK? UK & EEA (EU/EC) European Authorised Representative/Authorized Representative (UK Responsible Person) & CE Mark (CE Marking) consulting services
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.



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mdss.com

mdss.com mdss.com           
EU Authorized Representative Services For Medical Devices
MDSS USA is a EU Authorized Representative for Medical Devices, CE Mark, MDD, IVDD, AIMDD and European regulatory affairs.
Family of CP/M- and DOS-compatible multi-user multi-tasking operating systems. Multiuser DOS is a real-time multi-user multi-tasking operating system for IBM PC-compatible microcomputers. An evolution of the older Concurrent CP/M-86, Concurrent DOS and Concurrent DOS 386 operating systems, it was originally developed by Digital Research and acquired and further developed by Novell in 1991. Its ancestry lies in the earlier Digital Research 8-bit operating systems CP/M and MP/M, and the 16-bit single-tasking CP/M-86 which evolved from CP/M. When Novell abandoned Multiuser DOS in 1992, the three master value-added resellers (VARs) DataPac Australasia, Concurrent Controls and Intelligent Micro Software were allowed to take over and continued independent development into Datapac Multiuser DOS and System Manager, CCI Multiuser DOS, and IMS Multiuser DOS and REAL/32.The FlexOS line, which evolved from Concurrent DOS 286 and Concurrent DOS 68K, was sold off to Integrated Systems, Inc. (ISI) in July 1994.


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ce-mark.com

ce-mark.com ce-mark.com           
CE Mark, CE Marking Medical Devices, Machinery, ATEX, EU Authorized Representative
CE mark machinery, ce marking machinery, EU authorized representative for machinery, ATEX, PPE, ROHS, ROHS2.


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ce-marking.com

ce-marking.com ce-marking.com           
Need EC Rep/UKRP for both EU-27 & UK? UK & EEA (EU/EC) European Authorised Representative/Authorized Representative (UK Responsible Person) & CE Mark (CE Marking) consulting services
World leading Wellkang group offer UK & EEA (EU/EC) European authorised/authorized representative (UK Responsible Person) & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.


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easymedicaldevice.com

easymedicaldevice.com easymedicaldevice.com           
Home - Medical Device Regulation and ISO quality standard
Want to Master Medical Device Regulation & learn how to put a product on the market in Europe. Easy Medical Device is a platform for tools and resources for Regulatory Affairs, Quality Management, Regualtory Compliance. Learn how to choose your notified body or how the device regulation is different in other countries


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techintl.com techintl.com           
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mdssar.com mdssar.com           
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mdi Europa | CE Marking "Made in Germany" for Medical Devices
Germany based EU Authorized Representative "mdi Europa" helps small to medium sized manufacturers to enter european medical device market.


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axisinvest.com.au axisinvest.com.au           
Default Web Site Page


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advenamedical.com advenamedical.com           
Advena UK Ltd - Medical Device and Cosmetics Consultancy
We are a specialist medical device regulatory consultancy offering a UK Responsible person service, support on regulatory affairs, cosmetics responsible person, quality management systems, and in-vitro diagnostic consultancy.


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Medicines and Healthcare products Regulatory Agency
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .



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holdtechfiles.eu

holdtechfiles.eu holdtechfiles.eu           
Home Page - Do you need an Authorised Representative?
Act as Authorised Representative for non-EU manufacturers of CE marked products, and person to compile Technical Files on Machinery Directive Declarations.


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Laven offers a UK regulatory hosting platform which provides clients with the opportunity to conduct regulated activities as an Appointed Representative (AR), or, as a manager under MiFID or AIFMD without having to be directly regulated.



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