BMQR Certifications Pvt Ltd

BMQR Certification Pvt. Ltd. is known as the reliable CE marking provider throughout the world. The letters 'CE' on a product are the manufacturer's claim that the product meets the requirements of all relevant European Directives. Our CE marking is widely recognized by a large number of clients across the world. CE marking is mandated by New Approach Directives, which covers several products to be placed in the EU market and ensures that some must bear CE marking, as it is a legal requirement.


CE Marking On A Product

• It indicates to governments that the product can be legally sold within the European Union (EU) and the European Free Trade Area (EFTA).


• CE marking ensures that the product can move freely throughout the European Single Market.


• It indicates to customers that the product meets designated minimum safety standards and therefore a minimum level of quality.


• It promotes public health and safety.


• Enhances product credibility.


• It leads to improve sales and greater customer satisfaction.

The CE Marking Process

• Step 1: Identify the directive(s) that are applicable to your product. You can download these directives at free of cost from the web site of European Union.



• Step 2: Identify the conformity assessment procedure that must be taken. This could be self-declaration, involve testing, inspection or quality system assessment from a notified body or a combination of these. The conformity assessment procedure will differ depending on your product and the directive in respect of which you will get CE marking.



• Step 3: Determine the dates by which you must take action. This will be the date that the directive comes into force. The majority of directives are already in force. In these cases, it is an offence to place a product on the market without CE marking because it indicates a presumption of conformity with all relevant legislation.



• Step 4: Identify if there are any Harmonised European Standards applicable to your product. These are not always mandatory for manufacturers, although there is a presumption that conformity to these standards will give conformity with the relevant part of the directive. Manufacturers should follow harmonised standards, whenever possible or appropriate.



• Step 5: Ensure the product complies with all the essential requirements of the directive(s). Take appropriate measures to comply or identify existing data and test reports.



• Step 6: Identify whether independent assessment of your conformity to the directive or some aspects of it, is required from a notified body. This will be stated in the directive and is dependent upon the product you are getting CE marking for. You must not affix CE marking to your product until all necessary certifications have been obtained from the notified body.



• Step 7: Maintain technical documentation required by the directives. Your technical documentation should support your compliance with the requirements of the directive. It is essential to retain this documentation.



• Step 8: Prepare the declaration of conformity and the required supporting evidence. The declaration of conformity along with the technical documentation should be made available to competent authorities (EU Members) upon request.



• Step 9: Check that no other purely national requirements exist in the countries, where the product will be sold. These may include national standards, labelling or packaging requirements.



• Step 10: Affix CE marking on your product and/or its packaging and accompanying literature as stated in the directive