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1. Establishing contact First, we present ourselves and our range of services and get to know you, your company and your products. We then determine further procedures together. Early establishing of communication, e.g. as early as in the product development phase, allows for better coordination of the time schedule for the market launch of your product. 2. Quotation We will then prepare a quotation for you covering the services you request on the way to acquiring CE marking or RoHS Compliance. 3. Order After receipt of the order, we will discuss any open questions and coordinate the project handling together with you. 4. Technical documentation Prior to the audit, selected documents out of the technical documentation will be checked for plausibility and for conformity with the requirements of the directive. Documents will include: Technical Construction File
5. For all products Examination of the design dossier or EC type-examination. You submit to us the documentation on the product design (design dossier), included in the TCF, and we will check it for completeness and plausibility. Or we get your product re-tested and get the associated documentation. We will then issue a report on the test results. 6. Voluntary pre audit We will base the scope of the pre audit on your wishes. You will receive an audit report in which potential for improvements will be pointed out. 7. Review of the QM documentation The QM documents, such as the Quality Manual as well as relevant procedures, will be assessed by us prior to the audit, and you will receive a report on our findings. 8. Certification audit(Optional) Prior to the audit, you will receive an audit plan agreed on with you. During the audit, the operations in your company will be examined and thus the implementation and effectiveness of the requirements of the applicable directive and the relevant standards. In the process, we will particularly assess the conformity of the products with the essential requirements. The team of auditors always includes at least one expert on your product range. All relevant production sites are included in the scope of the audit. You will receive a detailed report on the performed audit that includes also advice for improvement. 9. Certificate/approval If the audit result is positive, you will receive an approval for the selected conformity assessment procedure. Afterwards, we will carry out surveillance audits every twelve months and a recertification audit after five years. 10. Declaration of Conformity You are now permitted to issue the declaration of conformity for your product, to provide them with the CE marking or RoHS Compliance mark, and to place them on the European market. Contact us - we are looking forward to hearing from you! |
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