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wellkang.com

Wellkang Consulting (Wellkang Consultant)

World leading consulting group are your one-stop global IT, marketing, export & regulatory compliance consultant! Offices in Europe, America & Asia

http://www.wellkang.com/

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Wellkang Ltd

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1.442●●●●●76300
1.442●●●●●11874
co●●●●●●●●@WELLKANG.COM

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Wellkang

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Lo●●on , England, W1G 9QR

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1.442●●●●●11874
su●●●●●@wellkang.co.uk

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Wellkang

Tec, Wellkang

Suite B,●●●●●●●●y Street

Lo●●on , England, W1G 9QR

UK

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1.442●●●●●11874
su●●●●●@wellkang.co.uk

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World leading consulting group are your one-stop global IT, marketing, export & regulatory compliance consultant! Offices in Europe, America & Asia
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Wellkang Consulting (Wellkang Consultant) | wellkang.com Reviews

https://wellkang.com

World leading consulting group are your one-stop global IT, marketing, export & regulatory compliance consultant! Offices in Europe, America & Asia

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INTERNAL PAGES

wellkang.com wellkang.com
1

Wellkang Consulting (Wellkang Consultant)

http://www.wellkang.com/index.html

Quick, Secure, Reliable and Affordable. Solutions to Your Success in World Trade! You want to export to the enormous. You want to get your product a " trade passport. For entering and being freely circulated in the entire EFTA and European Union (EU) single market (totally 30 countries)? You want to export to the ever growing. China market, with more than 20% of the world consumers? If you answer "Yes", then let Wellkang Consultants. A world leading consulting team can provide Q. CE Marking (CE Mark).

2

European Authorized Representative & CE Marking Consulting Service

http://www.wellkang.com/ce-mark

World leading Wellkang Tech Consulting group offers European Authorized Representative service for Medical Devices (MDD), Personal Protective Equipment (PPE), Low Voltage Electrical Equipment (LVD), Electromagnetic Compatibility (EMC), Toys, etc, your professional CE Marking authorised representative at www.-ce-marking.com - Your browser doesn't appear to support frames - please click here. To view the site.

3

Wellkang Online Shop: Accepting Credit Card/Check/Money Order/Bank Transfer

http://www.wellkang.com/shop

Click here for going to a page without frames!

4

Our clients: Fortune 500 and multinational companies as well as governmental bodies and international organizations

http://www.wellkang.com/our-clients.html

Governmental bodies and international organizations:. Advanced Science and Technology Institute, The Philippines - www.asti.dost.gov.ph. American Petroleum Institute, USA - www.api.org. Australian Department of Health and Ageing Library, Australia- www.health.gov.au. Bureau for Quality Supervision and Inspection of Henan Province, China. China-Britain Business Council - www.cbbc.org. China Textile Institute - www.cti.org.tw. CSEM (Swiss Center for Electronics and Microtechnology) - www.csem.ch. Mississip...

5

Brief introduction about the European Union (EU) and European Free Trade Area (EFTA)

http://www.wellkang.com/abouteu.html

Brief introduction about the. Unión Europea (UE). União Européia (UE). 15 Member States/Países de miembro/Países de membro/Payses du membre. Became member in 1995), Belgium. Founder Member in 1957), Denmark. FM 1957), Germany. FM 1957), Greece. FM 1957), Luxemburg. FM 1957), the Netherlands. FM 1957), Portugal. 1995) and United Kingdom (Great Britain). 10 New Member States. After May 1, 2004). 2004), Czech Republic. 2004), and Cyprus. 2 New Member States. After January 1, 2007). CE Marking and EU/EFTA.

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mhra.com mhra.com

MHRA registration: register your medical devices (MD/IVD/AIMD) with European Competent Authority & European (EU/EC) Authorized Representative service

http://www.mhra.com/index.html

Your Medical Devices ( MDs. In Europe with Competent Authority MHRA. UK Medicines and Healthcare products Regulatory Agency. As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. For Medical Device (MD).

mhra.com mhra.com

FAQs: Frequently Asked Questions about registration of medical devices (MD/IVD/AIMD) with European Competent Authority MHRA & European (EU/EC) Authorized Representative service

http://www.mhra.com/FAQs-frequently-asked-questions.html

Your Medical Devices ( MDs. In Europe with Competent Authority MHRA. UK Medicines and Healthcare products Regulatory Agency. As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. For Medical Device (MD).

ce-marking.com ce-marking.com

CE Marking (CE mark) EU/EC Declaration of Conformity: definition and required content (template)

http://www.ce-marking.com/required-content-for-CE-marking-EC-declaration-of-conformity.html

CE Marking (CE mark) EU/EC Declaration of Conformity: definition and required content (template). As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. The EC declaration of conformity. This declaration ...

eaarmed.com eaarmed.com

EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services

http://www.eaarmed.com/index.html

As of 21 March 2010. EEA European Authorised/Authorized Representative. Must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EEA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. You export to Europe? UL mark; China Compulsory Certification- CCC Mark. China RoHS compliance and solutions, etc. How can Wellkang help you? Wellkang's m...

eaar.org eaar.org

CE Marking (CE mark): manufacturer and its responsibilities: sub-contractor, authorized representative, importer, distributor, retailer, wholesaler, user

http://www.eaar.org/what-is-a-manufacturer.html

Looking for an EU/EC European Authorised/Authorized Representative. In Vitro Diagnostic Medical Devices in Europe by CE Marking. Specialists based in London/UK. Click here to get FREE Guide. CE Marking (CE mark):. Manufacturer and its responsibilities. Authorized representative, distributor, retailer, wholesaler, user, sub-contractor, own brand labeller, private labeller). The manufacturer has sole and ultimate responsibility for the conformity of the product to the applicable directives, whether he desi...

eaar.org eaar.org

Consulting & European (EU) Authorized Representative service for CE Marking, Machinery, PPE, LVD, EMC, Toy, at www.CE-marking.com

http://www.eaar.org/other-products.html

Are you ready for the new Machinery directive 2006/42/ec? Looking for an EU/EC European Authorised/Authorized Representative. Order to comply with NEW Machinery. Directive 2006/42/ec before 29 Dec 2009. Let the CE Marking specialists help you! Click here to get a Quote and Guide. Wellkang Group also offer CE marking Compliance Consulting service, as well as European Authorized Representative service for the following products:. Personal Protective Equipment (PPE). Low Voltage Electrical Equipment (LVD).

eaarmed.com eaarmed.com

Guide on IVD-In Vitro Diagnostic Medical Devices CE marking (mark) & European (EU) Authorized Representative service

http://www.eaarmed.com/medical-devices-in-vitro-diagnostic.html

As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. IVD-In Vitro Diagnostic Medical Devices: Conformity Assessment Routes. For all devices referred to in List A in Annex II. Set out in Annex V. For all...

eaar.org eaar.org

Guide on medical devices (MD/IVD) CE marking (mark) & European (EEA/EU/EC) Authorized Representative service

http://www.eaar.org/medical-devices.html

As of 21 March 2010. EEA European Authorised/Authorized Representative. Must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EEA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. FAQ/Q&A: Questions and Answers about CE Marking of Medical Devices. Is my product a Medical Device (MD). Or In Vitro Diagnostic Medical Device (IVD).

eaar.org eaar.org

Guide on IVD-In Vitro Diagnostic Medical Devices CE marking (mark) & European (EU) Authorized Representative service

http://www.eaar.org/medical-devices-in-vitro-diagnostic.html

As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. IVD-In Vitro Diagnostic Medical Devices: Conformity Assessment Routes. For all devices referred to in List A in Annex II. Set out in Annex V. For all...

eaar.org eaar.org

Services and Fees: European (EU) Authorized/Authorised Representative service for CE Marking: MDD, IVD, PPE, LVD, EMC, Toy

http://www.eaar.org/services-and-fees.html

Wellkang Offer Excellent Services At Very Competitive Prices! Looking for a European Authorised/Authorized Representative. In Vitro Diagnostic Medical Devices in Europe by CE Marking. Specialists based in London/UK. Click here to get FREE Guide. Compliance Consulting Service Fees. Compliance Consulting Service varies greatly from case to case, from product to product. Please click here. European Authorised/Authorized Representative Fees. Authorised/Authorized Representative service for Medical Devices.

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Wellkang Consulting (Wellkang Consultant)

Quick, Secure, Reliable and Affordable. Solutions to Your Success in World Trade! You want to export to the enormous. You want to get your product a " trade passport. For entering and being freely circulated in the entire EFTA and European Union (EU) single market (totally 30 countries)? You want to export to the ever growing. China market, with more than 20% of the world consumers? If you answer "Yes", then let Wellkang Consultants. A world leading consulting team can provide Q. CE Marking (CE Mark).

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Wellkang Ltd (London): your professional EC Rep: EU/EC European Authorised Representative/Authorized Representative!

Tels: 44(20) 32876300 / 30869438. Tel no. 44(20)79276844 and 44(20)79934346 are no longer in use. Member of Wellkang Group of Companies.

wellkang.org wellkang.org

Wellkang group of companies - www.wellkang.org

Wellkang group of companies - www.wellkang.org. Your browser doesn't appear to support frames - please click here. To view the site.

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