CE Marking Solutions

Access European Union Markets with the CE Mark

CE Marking is your ticket to EU market access.

We have helped countless manufacturers understand and meet the requirements of relevant New Approach Directives for CE Marking.

Put our advisory, testing, and CE certification services to work for you and allow us to guide you through every step of the CE Marking process:

1. Determine which directive(s) are applicable to your product
2. Fulfill the essential requirements
3. Establish a monitoring system
4. Establish an accident reporting system
5. Declaration of Conformity
6. Save the documentation for 10 years after a product has been placed on the market
7. Register with the appropriate governing body within Europe

Download Path to EU Market Entry:
CE Marking & CB Scheme

Notified Body Status

Intertek has five European Union-based Notified Bodies located across Germany, Sweden, France, Spain and the United Kingdom. We have the product expertise and full capability to test to a variety of directives, including:

• ATEX Directive (94/9/EC)
• Construction Products Regulation (CPR)
• EMC Directive (2004/108/EC)
• ErP Directive (2009/125/EC)
• Gas Appliance Directive (90/396/EEC) 
• In-Vitro Diagnostic Directive (98/79/EC)
• Low Voltage Directive (2006/95/EC)
• Machinery Directive (2006/42/EC)
• Medical Device Directive (93/42/EEC)
• PPE Directive 89/686/EEC
• Pressure Equipment Directive (PED and TPED)
• Regulation (EU) 2016/425
• RoHS Directive (2011/65/EU)
• R&TTE Directive (1999/5/EC)
• Toy Safety Directive 2009/48/EC