CE marking/certificate can be achieved through the following process:

Manufacturers can provide Self-declaration of the products that fulfil the standard requirements. Because, there are no third-party audits or other involvement of external bodies, it is not a recommended best practice.

For non-risky products (Nonmedical) items are certified by a third-party body. The self-declaration form signed by the manufacturer or importer will be attested by the third-party provider.

These certificates are issued by EU notified bodies only. The products are tested throughout, based on the requirements post clearing the test, technical documentation is to be defined on the product.

The products are categorized based on their purpose of use and application in real life.

Some of the product classification categories are

• 2000/9/EC – Cableway installations
• 2014/35/EU – Low Voltage (LVD)
• 2006/42/EC – Machinery (MD)
• 93/42/EEC – Medical Devices (MDD)
• 2014/30/EU – Electromagnetic Compatibility (EMC)

CE Marking Services ensures your product is well built and quality is not compromised at any stage of production. It will testify the fact that your product is full proof and is of top-class quality.

The European Conformity Standard will help you to monitor the product performance continuously and indicate any deviations. Necessary actions are taken to mitigate any non-conformity to product quality and standards.

Our team of expert will help you through the CE Marking Certification process and guide you have a hassle-free process.

We have tie-ups with industry-leading Third-party notified bodies who will conduct full-fledged CE marking audits and certification.

Talk to our experts right away!