CE consulting - KERN helps with CE labelling

We offer our customers a comprehensive CE management service in accordance with the applicable CE directives:

• Testing and preparation of the risk assessment
• Testing and preparation of the CE Declaration of Conformity and Declaration of Incorporation
• Workshops and webinars for CE conformity assessment procedures
• Introduction and training of CE software
• Assistance and support with communication with notified bodies such as TÜV
• Standards research, e.g. for new products
• Review of product approvals, required documentation, documents such as EMC tests
• Checking market and target group requirements
• Support and optimisation of internal CE processes

Our employees use the following software to support them in preparing the risk assessment and other applicable documents:

• WEKA Manager
• SafeExpert

The following contacts are considered for the creation of documents and communication with external bodies in the product life cycle:

• CE coordinators
• Authorised documentation officer
• Quality management
• Design and development managers

We support our customers with approvals, tests and acceptances of products, machines, etc. For example, in communication with:

• TÜV Süd
• VDE
• VDI
• test laboratories
• Dekra
• Federal Network Agency
• FDA (USA)
• BfArM medical devices

In addition, we can customise the processes required for certification purposes through the CE coordinator. The technical documentation is also important for the preparation of test certificates and certificates of performance. This is where the required acceptance documents from the departments come together and are assessed.