The initials “CE” stand for Conformity Europeans, which is French for “European Conformity”. The CE Mark, which is affixed to a product or its packaging, is considered proof that a product has met the requirements of the harmonized European standard . CE marking on a product indicates to all authorities that the product is in compliance with the essential health and safety requirements of all directives that apply to the product.
The first step to compliance is determining which directives apply to the product. A product may be regulated by more than one directive. The CE mark does not disclose which directive(s) or standards apply to the product, nor will it indicate the method of conformity assessment used to bring the product into compliance. This information is provided by other accompanying documents, such as the Declaration of Conformity. The Manufacturer or the Authorize representative affixes the CE marking to the product. It is not affixed by a Notified Body.
We will do a FREE GAP analysis of your organisation with respect to CE Marking Standard and give you a quote.
Once you have agreed to our quotation, Our team will provide the required trainings to you and will complete the documentation work required for CE Marking certification.
We will then conduct a pre assessment audit to ensure that you organisation meets the desired certification requirements.
We will provide assistance during final certification audit to ensure that your organisation achieves certification successfully!
We are a quality conscious organisation and believe in Total Customer Satisfaction. So if you are 100% satisfied and happy with our service, make payment to us.