Who We Serve
What we do:
CE Marking
The CE mark indicates that your product is in compliance with the European product legislation. It is mandatory for all manufacturers whose products fall within the applicable CE Directives and Regulations to get CE marking before they can access the European market. If a company wants to market the product under its own name, the company will be seen as the legal manufacturer and bear the same responsibility as the original equipment manufacturer (OEM) and must apply the CE marking itself.
Obtaining CE marking can be a lengthy and complicated process. Herein, time and knowledge of regulations must be taken into account during the process. As well as the applicable testing facilities and risk assessment that are required to complete this CE certification.
Our CE mark experts will guide you through all processes and perform testing in order for your products to be able to obtain CE marking. As your full-service compliance partner, we will ease this lengthy and complicated process of obtaining the CE mark.
- CE Marking for Machinery
- CE Marking for Electronics
- CE Marking for Medical Device
- ATEX 114
- General Product Safety products
Compliance for different Markets
To be able to enter a market, your products must be in compliance with the national safety product legislation of your preferred market. This can be done through measures which are used to assess and certify the compliance with said legislations.
Obtaining product and service compliance can be a complicated process. For this, it is important to consider which products require which certification. Herein, time and knowledge of regulations must be taken into account during the process to complete the compliance process.
Certification Experts will support you throughout the entire process, from defining your requirements to conducting product testing, ensuring your products achieve full compliance. As your compliance partner, we’ll streamline this complex and time-consuming procedure.
- Europe (EU) – CE Marking
- United Kingdom (UK) – UKCA Marking
- United States of America (USA) – US and UL Compliance
- Canada – Canadian and CSA Compliance
- China – Chinese and CCC Compliance
- Other markets – International Compliance and CB Scheme
Authorised Representation
An Authorised Representative (AR) can be of service for manufacturers based outside of the EU and the UK who want to sell their product on the EU and UK market. An Authorised Representative acts on behalf of the manufacturer and ensures that the products being sold on the market comply with the applicable product compliance legislations, meaning they provide you with Authorised Representative services. This concerns products that are sold either directly, via e-commerce (online), or through a fulfilment service provider.
Whether you want UK or EU Authorised Representative services, AR Experts has both the knowledge and the experience to fulfil this role for you.
- EU Authorised Representative (EU AR)
- EC Rep (EU AR for Medical Devices)
- UK Authorised Representative (UK AR)
- UK Responsible Person (UKRP for Medical Devices)
Quality Management Systems
Quality Management System (QMS) is implemented in order to help an organisation to continuously develop the quality of their products and services. Due to this, it is important to keep in mind that when building a quality system, it must conform to the requirements and guidelines set in a standard or regulation, especially if one plans to have a QMS audit.
Our team of experts can determine which QMS is necessary for your organisation in relation to your products and or services within your industry of choice and then guide you through this process.
- ISO 13485
- ISO 9001
- QMS according to article 10 of the MDR
Safexpert
Explore the reliability of Safexpert, our extensively tested software designed for CE marking and Risk Assessment in alignment with the Machinery Directive and the Low Voltage Directive. With Safexpert, you gain access to tailored modules that facilitate seamless collaboration within your team, aiding in safety-centric project management and navigating the complexities of standards and EU directives.
- ISO 12100 compliant
- Get the CE Marking
- Optimize your workflow
- Connect your Team
Your next global market is waiting Let us help you unlock it
Full-service product compliance
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