Ce Marking Brochure v2.3 in en 0421
Ce Marking Brochure v2.3 in en 0421
Ce Marking Brochure v2.3 in en 0421
Introduction
The European Union is the world’s largest trading block and consists of some 500 million consumers. It’s therefore no surprise that
organizations from around the world choose to access this important market. CE marking is mandatory for many products placed
on the European market, so it’s crucial that organizations understand the steps they need to take as they navigate this
regulatory landscape.
What is CE marking?
CE marking on a product is the manufacturer’s declaration that their product complies with the essential requirements of all the EU
Directives/ Regulations that apply to it. It is a legal requirement to place certain products on the market in the European Union.
The requirements for CE marking differ across all the Directives and Regulations and may also vary for different products within a
Directive/Regulation. Depending on the product, CE marking could purely require a technical file to be compiled, or it could be a
more involved process requiring the product to be submitted for regular independent scrutiny.
Requirements for CE marking range from a manufacturer’s declaration, up to mandatory full Notified Body assessment of the
product and manufacturing controls. BSI can work with you throughout this process, so when you choose BSI, you can be confident
that you’re working with a trusted brand with a strong international reputation and world-class expertise in product certification.
Services to support your CE marking
BSI can work with you to affix the CE marking and we are a Notified Body for the following:
Directives such as Low Voltage Directive (LVD) and Electro Magnetic Compatibility (EMC) and the Machinery Directive (excluding
Annex IV products) are self-declaration and do not require the services of a Notified Body, but we are still able to deliver
services such as issuing reports to clients which can be used to provide evidence of compliance.
*Note: CE marking services for Medical Devices and IVD’s are operated by BSI Regulatory Services
At every step of the CE marking process we are committed to delivering an excellent service and working with you so that you can
bring new products to market, innovate, comply and build resilience in your organization.
• Standards identification
• Technical file evaluation
• Gap analysis
• Initial type testing
• Type examination
• Quality system assessment
• Factory production control (FPC) system assessment
• EC certificate or certificate issue (where applicable)
• Surveillance of product and quality system or FPC
• Verification certificates
The CE marking process with BSI
Our step-by-step CE marking process will take you from your application with BSI through to a certificate to support your
CE marking declaration being issued to your organization. Although CE marking requirements vary from Regulation to Regulation,
and even within Regulations, our team of trusted experts understand these requirements and can work with you at every stage, so
you can achieve compliance and remain resilient. From the moment your application is submitted to the moment the CE marking is
affixed to your product we are here to work with you in a partnership of trust.
Step 5B Self-declaration
The manufacturer may be able to test their own products and / or Factory Production Control (FPC).
Step 6 CE marking
You affix the CE marking to the product and produce an EU Declaration of Conformity. (Also known as
Declaration of Performance for construction products).
Phone:
Email: HMĦNHM@bsigroup.com