Access the European Market with Confidence

CE Marking is mandatory for many products sold in the European Economic Area. It indicates that a product meets EU safety, health, and environmental protection requirements. QPS helps manufacturers and exporters navigate the complex CE marking process, from identifying applicable directives to preparing technical documentation.

Who Needs CE Marking?

Manufacturers and exporters of machinery, electrical equipment, medical devices, construction products, toys, personal protective equipment, pressure equipment, and other products covered by EU directives planning to sell in the European market.

Key Benefits

  • Legal access to European Economic Area markets (30+ countries)
  • Enhanced product credibility and market acceptance
  • Simplified entry to markets recognizing CE Marking
  • Demonstrated compliance with EU safety standards
  • Reduced liability risks in European markets
  • Competitive advantage over non-certified competitors

Our Process

1

Directive Identification

Identify applicable EU directives and harmonized standards for your product category.

2

Product Assessment

Conduct conformity assessment, testing, and gap analysis against essential requirements.

3

Technical Documentation

Prepare technical file, Declaration of Conformity, user instructions, and labeling.

4

Notified Body & Marking

Coordinate with Notified Bodies where required and guide CE marking application.

Product Categories We Support

  • Machinery Directive (2006/42/EC)
  • Low Voltage Directive (2014/35/EU)
  • Electromagnetic Compatibility (2014/30/EU)
  • Medical Devices Regulation (EU 2017/745)
  • Construction Products Regulation (305/2011/EU)
  • Toy Safety Directive (2009/48/EC)
  • Personal Protective Equipment (EU 2016/425)
  • Pressure Equipment Directive (2014/68/EU)

Export to Europe with Confidence

Let QPS guide you through the CE marking maze.

Get Free Consultation →