As a Notified Body, we can evaluate all products in the scope of the Directive through the following two-stage process,:
1) Type Examination – Laboratory evaluation of the product to ensure it complies with the essential requirements of the Directive (typically by using an EN standard). This may be at one of our laboratories, your site, or a partner laboratory.
2) Production Surveillance – Ongoing assessment of production processes to ensure the essential requirements continue to be met.
Contact us today to start your journey to certification where we can help you to meet the requirements of the Directive.