World leading Wellkang Tech Consulting group offer EEA (EU/EC) European authorised/authorized representative & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
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Tec, Wellkang
Suite B,●●●●●●●●y Street
Lo●●on , England, W1G 9QR
UK
View this contact
Wellkang
Tec, Wellkang
Suite B,●●●●●●●●y Street
Lo●●on , England, W1G 9QR
UK
View this contact
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EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services | ce-marking.com Reviews
https://ce-marking.com
World leading Wellkang Tech Consulting group offer EEA (EU/EC) European authorised/authorized representative & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
ce-marking.com
What is CE Marking (CE mark)?
http://www.ce-marking.com/what-is-CE-marking.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. Is CE Marking (CE Mark)? What is CE Marking (CE Mark)? As shown on the top of this page. The letters " CE. Are the abbreviation of French phrase " C. In 1993. "CE Marking" is now used in all EU official documents. "CE Mark" is also in use, but it is NOT the official term. CE Marking on a product ensures the free move...
CE Marking (CE mark): manufacturer and its responsibilities: sub-contractor, authorized representative, importer, distributor, retailer, wholesaler, user
http://www.ce-marking.com/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...
EC Rep: What is EEA/EU/EC European Authorized Representative (Authorised Representative)?
http://www.ce-marking.com/authorised-representative
As of 21 March 2010. EEA/EU/EC 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 (EU/EFTA) authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. As of 21 March 2010. EEA/EU/EC European Authorised Representative (Authorized Representative). Commercial representatives of the manufactu...
EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services
http://www.ce-marking.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...
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 ...
TOTAL PAGES IN THIS WEBSITE
21
WEEE registration & WEEE compliance
http://www.weeeregistration.com/index.html
Sell EEE-Electronic and Electrical Equipment to Europe? Are you ready for WEEE registration and WEEE compliance? European WEEE Directive 2002/96/EC. On Waste of Electronic and Electrical Equipment has been transposed in national law/legislation and become effective. The manufacturers became financially responsible for the compliance to the WEEE directive since 13 August 2005. Failure to comply with the WEEE directive and national WEEE regulations will lead the manufacturers to prosecution. Improve the en...
WEEE registration & WEEE compliance
http://www.weee-guide.com/index.html
Sell EEE-Electronic and Electrical Equipment to Europe? Are you ready for WEEE registration and WEEE compliance? European WEEE Directive 2002/96/EC. On Waste of Electronic and Electrical Equipment has been transposed in national law/legislation and become effective. The manufacturers became financially responsible for the compliance to the WEEE directive since 13 August 2005. Failure to comply with the WEEE directive and national WEEE regulations will lead the manufacturers to prosecution. Improve the en...
TOTAL LINKS TO THIS WEBSITE
348
CE-markeren.nl
Deze site wordt u als dienst aangeboden door:. Is de app een medical device? In welke klasse valt de app? Wat moet er in het technisch dossier? Check hier uw app. Het zat er al een tijd aan te komen, maar vanaf 1 januari 2014 is het zover: de Inspectie voor de Gezondheidszorg (IGZ) is begonnen met het streng controleren of medische hulpmiddelen wel correct CE-gemarkeerd zijn. Maar wanneer is dat dan het geval? En wat houdt CE-markering eigenlijk in? Met deze vragen en meer helpen we u op deze website.
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ce-marking-authorized-representative.com
Martin Biggs Associates ~ GBM Authorized Representative ~ CE Marking European Authorized (Authorised) Representative Services ~ Professional CE Marking (CE-Mark) Consultants
REGULATORY AFFAIRS – REIMBURSEMENT. Martin Biggs Associates is a healthcare / regulatory affairs consultancy with over 30 years experience. We can provide advice and assistance with European, Australian, South African, Chinese and US – FDA authorization of drugs, devices, drug/device combinations, IUDs, and cosmetics. Drug / Medicinal Product registration in Europe and other territories. CE marking / Medical Devices. FDA Drug and Device registration. In vitro Diagnostics registration. And a member of the...
ce-marking-certification-kolkata.cemarkingkolkata.com
CE Marking
The CE marking shall be attached only by the manufacturer or his approved representative. CE marking is compulsory, but only for those products which are covered by the scope of one or more of the New Approach Directives. Welcome to CE Marking. What is CE Marking? Benefits of CE Marking. Need of CE Marking. CE Marking Desinged By : Zoomla Infotech.
ANKA GLOBAL www.ankaglobal.com ProductServices
ANKA GLOBAL www.ankaglobal.com ProductServices. Ce marking,ce certificate, ce certification, ce certificate conformity,ce,ce mark,ce notified body,notified bodies, machinery directive, lvd test, lvd directive, emc test, emc directive, machinery ce, construction directive, PAD directive, ce markalama, ce belgesi, ce markası. 11 Nisan 2011 Pazartesi. ANKA GLOBAL Conformity Assessment Services Ltd. www.ankaglobal.com. Shortly, it is quite important not to see CE mark as quality mark. CE mark is the assu...
EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services
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...
www.ce-marking.es
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EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services
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...
EC Rep: EEA (EU/EC) European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services
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...
www.ce-marking.info – このドメインはお名前.comで取得されています。
One-stop CE Marking (CE Mark) Information Source: Everything you need to know about CE marking - World's most comprehensive multi-lingual information guide on ce conformity marking. CE-Marking, CE Mark or EC Mark?
In Vitro Diagnostic Medical Devices in Europe by CE Marking. Specialists based in London/UK. Click here to get FREE Guide. The "Trade Passport to Europe" for non-EU Products. Your One-Stop Information Source -. Here you can find everything you need to know about CE marking:. CE mark approval, CE testing, CE mark requirements, etc. This website is the property of Wellkang Tech Consulting. Including totally 30 EEA* countries. And it is often referred as the "Trade Passport to Europe" for non-EU products.
