What is CE approval?

CE approval is a mark that confirms that a product complies with applicable European directives and standards. It is mandatory for many products within the European Economic Area (EEA) and enables the free movement of goods. The CE mark indicates that the product is safe and poses no health risks.

What needs to be considered for CE approval?

Manufacturers must complete several steps and requirements to obtain CE approval. First, they must check which EU directives and regulations apply to their product. This includes identifying the harmonised standards that specify specific safety and performance requirements. A risk assessment must then be carried out to identify potential sources of danger and take appropriate measures to mitigate risks.

The next step is to prepare the technical documentation. This must contain detailed information about the design, manufacture and operation of the product, including test reports and evidence of compliance with the relevant standards. A declaration of conformity in which the manufacturer confirms compliance with the EU requirements is also required.

If necessary, the product must be tested and certified by a notified body, especially in the case of higher risks. Finally, the CE mark must be affixed to the product in a clearly legible manner. The EU declaration of conformity is kept in the technical documentation. Only then may the product be placed on the market.

IBC and CE approval

The CE mark guarantees that certain types of IBCs (SCHÄFER heating containers or SCHÄFER SLC aseptic containers) are safe. This not only protects the health of users and consumers, but also helps to prevent accidents and environmental damage. In addition, CE approval facilitates the free movement of goods within the European Economic Area.