Quality Certificates

CE Mark

The CE Mark is applied to products regulated by European Union health, safety

and environmental protection laws. The CE Conformity Mark is applied to

products that fall within the scope of New Approach Directives (Technical

regulations), of which there are approximately 23. CE Conformity Mark is

mandatory for manufacturers who want to market their products in the

European Market. Otherwise, it is impossible to produce and sell their products

in this market. Products that do not comply with technical regulations

(directives) cannot be placed in the markets of European Union member states

and EU candidate countries that have harmonized the relevant legislation, as

well as Norway, Iceland and Liechtenstein. If the product meets the conditions

in the directive and carries the CE Conformity Mark, these countries will not

impose bans and restrictions on the entry of the product into the market or

offering it to the consumer. Therefore, the CE Conformity Mark is the passport

of a product in Europe.

ISO 9000 Quality System and Certificate

ISO 9000 series is one of the necessary applications for compliance with the European Union. These standards, published in 1987, began to become widespread especially in 1990 and later. This document, which indicates that Total Quality Management, the most modern application of quality, has been implemented at an acceptable level, has become an indispensable element of reliability and competition for companies.

The ISO 9000 series sets out quality assurance standards that can be applied to any small, medium or large-sized business or service provider, can be used for any existing system and contributes to the business reducing its internal costs, increasing its effectiveness and efficiency, and improving overall quality and quality. It is a step towards continuous improvement. It does not include ISO 9000 series product standards. Each document in the ISO 9000 series defines a quality model for different applications.