According to the provisions of the EU directive, we can test the implementation of CE programs into the following five steps:

      The first step: the implementation of the sample test. That is, R & D stage for sample inspection and testing. According to the different requirements of the Directive, some product categories tested by the companies themselves, or commissioned, additional testing of some products must be made by the European Union announced the certification body (Notified Body, Competent Body) implemented. The former is the harm is low and clear product testing standards, such as toys, common household appliances, computer products, while the latter is for high hazard, the wider products such as personal protective equipment, medical supplies, communications products.

      Step Two: Create a "technical file." "Technical File" is the EU directive is very important matter, its purpose is to require companies to prepare adequate technical information and proof, the competent authority for the checks, or use in the event of litigation. Different instructions, for "technical file" requirement slightly different, but basically consists of three aspects: (1) product technical information, (2) test report, (3) manual. If the test according to instructions provided by the certification bodies, the "technical file" must include the agency issued the "EC type approval certificate."

      The third step: the implementation of production quality assurance system. The first and second step, the main requirement is for a single sample, the next question is how to ensure production of products and samples tested have the same quality? So the instructions require companies to develop for mass production appropriate quality assurance systems. This quality assurance system, which can be