Most products require CE marking to be sold in the EU. This marking is proof that the particular product has undergone assessment and complies with the health, safety, and environmental protection requirements. Therefore, as a manufacturer, ensure your products are as per the necessary requirements before you get the CE marking. For instance, if you manufacture medical or electronic devices, you need the CE mark to ensure the devices sell in countries in the European Economic Area (EEA). Notably, once the components of the products are certified, you may still need certification for the overall device. After all, when two or more systems that are already CE-marked may not automatically result in a compliant device.