The eulaboratory S.p.A. is accredited by TRA (Tested Recognition Arrangements) - international accreditation body
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The legislative intricacies of the European Union: in order to trade products in the EU, it is essential to understand the different health and safety requirements that your product must comply with.
The eulaboratory specialty is to fully support you in knowing, understanding and master all the Directives and Regulations of the EU.
Directives and Regulations are two different thing in the EU world, and figure out this topic it's very important for the CE marking and all the certification that may concern your company, industry, servie or product.
An EU Regulation is binding legislative act that have direct implications for all member states. They are applied in their entirety across the EU, meaning that they are directly applicable in every member state and can be immediately enforced through law like any piece of local legislation.
An EU Directive is a legal act which requires member states to accomplish a particular set of goals without dictating the means to do it. In other words, it outlines certain rules which must be met, but each member state decides how to ensure compliance through national laws. Directives specify an exact date by which they must be implemented (or transposed) into national law.
As accredited body, The eulaboratory offers tests and certifications to prove the conformity of any product with its European requirements, in order to place the product in the market with all the winning features for Europe and the rest of the world.
