European Union || International Approvals

European Commission directives define the “essential requirements”, e.g., protection of health and safety that goods must meet when they are placed on the market.

Regulations

The CE marking process:

1. Identify the applicable directive(s) and harmonised standards applicable to the product

2. Identify the applicable product specific requirements of the directive(s)

3. Identify an appropriate route to conformity and whether independent conformity assessment is required from a Notified body

4. Assess the product’s conformity

5. Compile the required technical documentation

6. Make an EC Declaration of Conformity and affix the CE mark

 

 

Conformity Mark

SIQ Services

SIQ performs conformity assessment according to the requirements of various European directives and carrying out the tasks of Notified Body with identification number 1304. SIQ issues also Attestation of Conformity for CE marking.

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