CE Certification, CE Consultant, CE Mark, CE Consultancy

CE Certification

The following simple steps are involved
STEP 1: Identify Applicable "DIRECTIVES"
STEP2: Identify Applicable "Conformity Assessment Module"
Although CE Marking follows the Self Declaration principle, depending upon product complexity and risk to human life, various conformity assessment module are prescribed:-
Module 'A' (Internal Production control).
Applicable for products falling under EMC and Low Voltage Directives. Manufacturer tests the product from third party. After compliance with the tests, his production process ensures continued conformance. He maintains "Technical Documentation" as a proof of compliance. There is No mandatory involvement of European Lab (i.e. Notified Body).
Module 'B' to 'H'
Mandatory involvement of European Lab is required which issues "Type Examination Certificate", certifies documentation (called "Technical Construction File"(TCF) and carries out inspections.
STEP3: Identify Applicable "Standard"
STEP4: Test one sample of the product. Either yourself or from test lab.
STEP5: Compile "Technical Documentation"
STEP 6: Sign the EC "Declaration of Conformity"
STEP 7: Affix "CE Mark" on the product.

Should you require assistance in CE Marking of any products, consultancy for CE Mark, CE documentation and located in Bangalore, Chennai or Hyderabad please drop a mail to shakti@gqsindia.com or call +91 9845313910 or +919845078743

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Expertise spread over CE Certification, CE Consultant, CE Mark, CE Consultancy of Medical Equipments, Hand Held devices, Aeronautical parts, Machine Tools, Power tools, Electrical panel boards,Transformers, Toys, Engineering parts and a whole lot of products under various direcitves.