CE marking

In Vitro Diagnostics or Medical Devices that are placed on the European market must meet the requirements of their respective European Directives and Regulations. Conforming products will receive the CE mark as the evidence of compliance.

Qarad offers a complete list of services to assist manufacturers in obtaining the CE mark for their products.

Why Qarad?

Qarad’s consultants have more than 30 years experience in the IVD and Medical Device Industry. Therefore they offer a professional and cost-effective approach to CE-marking. They develop the right strategy and provide hands-on assistance in every step of the regulatory process.

7 steps to CE mark

Contact us for more information