Product certification provides proof that, before its market release, agiven product has been comprehensively tested by a third-party accredited body that is independent of both the seller and the manufacturer, to ensure that it complies with the requirements laid down in European and/or international directives.
Certification can be mandatory or voluntary. In the former case, it is a legal requirement, and the product cannot be commercialised unless it first undergoes all the necessary checks by an accredited body. This category includes the most complex products, such as gas appliances, medical devices, pressure equipment and certain construction products.
In the case of voluntary certification, manufacturers decide, of their own volition, to have their products checked by a third-party body so as to provide an additional guarantee of their quality and to equip the market with an effortless, transparent aid to making purchasing decisions.
IMQ can operate in both these areas. For mandatory certification, it acts in its capacity as a notified body for European reference directives (CE Certification 0051) and certain international directives. For voluntary certification, it operates as a third-party certification body accredited to issue the IMQ mark and other voluntary marks, both European and international.
The voluntary certification system proposed by IMQ is the most comprehensive system and provides a long-term guarantee. In addition to type tests on product samples and auditing of the manufacturer’s quality assurance system , the IMQ scheme also involves production monitoring once the product has been commercialised.