CE marking
implement safely and efficiently

From risk assessment to the declaration of conformity: we support companies through every stage of the process to ensure CE marking complies with the law and to secure successful market access in Europe.

CE marking
implement safely and efficiently

From risk assessment to the declaration of conformity: we support companies through every stage of the process to ensure CE marking complies with the law and to secure successful market access in Europe.

CE marking for products, machinery and technical installations

Compliance with legislation for the European market

The CE marking is a prerequisite for the sale of many products within the European Union. It confirms that the applicable requirements regarding safety, health and environmental protection are met. Without proper CE conformity, this may result in sales bans, market surveillance measures or liability risks.

We support companies in implementing the entire CE process in a structured and efficient manner. From analysing the relevant directives through to risk assessment and technical documentation, you receive practical support from a single provider.

Our services in the field of CE marking

Comprehensive support for manufacturers and distributors

Identification and assessment of potential hazards as the basis for a conformity assessment in accordance with standards.

Preparation and verification of EU declarations of conformity and other necessary supporting documentation.

Compilation and verification of the technical documentation as the basis for a legally compliant CE marking.

Identification of the relevant European directives, regulations and harmonised standards for your product.

Support in working with testing laboratories, certification bodies and notified bodies.

Practical training courses for specialist departments, project teams and CE officers.

Prepare for the Machinery Regulation 2027 in good time

From January 2027, the requirements of the Machinery Regulation (EU) 2023/1230 will become binding. For many companies, this will necessitate adjustments to risk assessments, technical documentation and digital operating instructions.

We can help you prepare your existing processes and documentation for the new requirements at an early stage and minimise potential risks.

Why professional CE consultancy is worthwhile

The requirements for CE marking vary depending on the product, sector and target market. Professional support helps to avoid mistakes and reduce the workload for in-house teams.

Your benefits:

Greater regulatory compliance
Faster time to market
Clear project structures
Support with liaising with public authorities and inspection bodies
Reduced liability risk
Relief of pressure on internal resources

This is how a CE project works

A structured approach to compliance

1
Analysis

Assessment of your product and the relevant directives and standards.

2
Risk assessment

Assessment of potential hazards and identification of necessary protective measures.

3
Documentation

Preparation or review of all necessary technical documentation.

4
Conformity assessment

Carrying out the necessary verification and testing procedures.

5
CE marking

Completion of the procedure, including the declaration of conformity and the marking of the product.

For which companies is CE consultancy relevant?

Our CE experts support companies in the following sectors, amongst others:

  • Mechanical and plant engineering
  • Electrical engineering
  • Medical technology
  • Automation technology
  • Consumer goods industry
  • Industrial goods manufacturing

A professional assessment of CE requirements is particularly recommended for new developments, product modifications or when entering new markets.

Frequently asked questions about CE marking and conformity assessment

Frequently asked questions and answers

The CE marking indicates that a product complies with the applicable European Union requirements and may be placed on the market within the European Economic Area.

The obligation depends on the relevant European directive or regulation. This applies, amongst other things, to machinery, electrical equipment, medical devices and numerous other product groups.

Responsibility generally lies with the manufacturer or the distributor of the product. They must demonstrate conformity and provide the necessary documentation.

Depending on the product, this may include risk assessments, technical descriptions, test reports, operating instructions, declarations of conformity and other supporting documentation.

Risk assessment analyses the potential hazards of a product and defines measures to mitigate those risks. For many products, it is one of the key requirements for CE conformity.

The new Machinery Regulation replaces the previous Machinery Directive and introduces additional requirements, for example in the areas of digitalisation, cybersecurity and risk assessment.

Depending on the individual case, this may result in sales bans, product recalls, fines or liability claims.

The time required depends on the type of product, the current status of the documentation, the testing requirements and the regulatory complexity. An initial analysis will quickly clarify the scope of the work.