Achieving CE marking is essential for manufacturers aiming to distribute products within the European Economic Area (EEA). It signifies that a product complies with the relevant European directives and regulations.
CE marking is the manufacturer’s declaration that their product meets the essential requirements of all applicable European directives. This marking is mandatory for specific product categories, including medical devices, machinery, electrical equipment, and personal protective equipment. Affixing the CE mark allows for the legal sale of products within the EEA, facilitating access to a market of over 500 million consumers.
We support certification for the following regulations and directives:
- Construction Products Regulation (CPR 305/2011)
- Structural Steel and Aluminium (EN 1090 under CPR)
- Gas Appliances Regulation (EU 2016/426)
- Marine Equipment Directive (MED 2014/90/EU)
- Pressure Equipment Directive (PED 2014/68/EU)
- Personal Protective Equipment (PPE) Regulation (EU 2016/425)
- Medical Devices and IVDs
- Lifts and Lift Components – Lift Directive 2014/33/EU
- Low Voltage Directive (LVD 2014/35/EU)
