Atlantic Bridge was formed in 1995 to help businesses meet the growing requirements of European Regulatory Compliance. The company has assisted many companies from North America as well as companies within Europe, Australia, The Middle East, and Asia.

 Now that the UK has left the EU Atlantic Brdige Limited is using their expertise and exprience to assist Companies throughout the world with the UK requirements for UKCA marking which will apply to most products before 31/12/2024 and for medical by July 2024. In additional we are able to act Authorised Representative for other products where an Authorised representative is required but the product does not fall within the UKCA Markingrequirements.

We can act a your UK Authorised Representative (non-medical) or Responssible Person (medical).

Our previous expertise included assisting with CE Marking, installing quality management systems, assessing product risks and general product safety, advising on Workplace Health and Safety, and acting as an Authorised Representative for Europe. We still maintan the ability to asisst UK businesses with CE marking but do not normally not offer this service outside of the UK but have contacts in the EU who can assist,

For many UK Product Regulations  Non-UK based manufacturers must appoint either a UK based Authorised representative or Responsible Person (Medical Devices)  to continue to meet UK regulatory requirements. For some they can employ their importers. Each Importer must take full responsibility for UKCA marking and hold copies of the Manufactureres Technical Files which may include any IPR they hold. This can lead to copy-catting their products. Atlantic Bridge can take the responsbility for holding the relevant documents secure and only make them available to the regulatory authorities removing the risk of importers being able to replicate the products as their own.

Atlantic Bridge also offers a wide range of training to companies needing assistance with UKCA Regulatory Compliance. Atlantic Bridge can help you achieve UKCA Marking for Construction Products, Machinery, Medical Devices, Electrical and Electronic Equipment,  Personal Protective Equipment and most other products previously covered by the European New Approach Directives but also now covered by UK Statutory Instruments for UKCA Marking.

We have experience of software used as a medical device as well as standard software quality systems.

If you are looking for help with:

• UKCA  Marking
• Management Systems to ISO 9001 or 13485 (Medical Devices) - Quality
• Management Systems to BS EN ISO 14001 - Environmental

then send an email to This email address is being protected from spambots. You need JavaScript enabled to view it. to see how we can help you.

Registered Office:  Atlantic House, 19 Willowside, Woodley, Berkshire RG5 4HJ UK
Registered in England Number 3102076
VAT GB 642 0739 51