Products to be sold in the European Union (EU) that come under European Directives must carry the specified CE mark – it is a legal requirement.
Compliance can be complex as CE marking requirements vary between Directives and even within Directives.
At BSI, we have a team of experts who understand precisely what each Directive requires for each product – to make your life easier.
In many cases the compliance route will require you to use a Notified Body to assist with your certification. BSI is a Notified Body for 17 European Directives and offers one of the most comprehensive certification services in the world.
European New Approach Directives provide a range of compliance routes for your product and show you, usually in a modular format, the available routes to compliance. You must decide which route is the best fit for your company and follow your chosen route as detailed in the Directive.
BSI works in close partnership with our clients to help you through the process of achieving compliance and affixing the CE mark to the product. We can help you choose the best and most appropriate compliance solution for your product.
However simple or complex your needs, BSI is the only name you need to know when considering CE marking.
Next Steps
For further information about CE Marking for medical devices, please request a quote or contact us.
For further information about CE Marking for all other products, please visit our Global website and request further information.
