Your UK Representative.

We help get your products approved for UK and EU markets. As an independent UK based Responsible Person or Authorised Representative with 30 years of experience, we can help you with CE/UKCA marking so you can sell with confidence.

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We're based in the UK

Assist with the provision of technical documentation required by UK legislation.

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We're based overseas

Act as your responsible person for the supply of medical devices and products to the UK.

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Resources

Medical device requirements

Read about device requirements that manufacturers must abide by.

UK regulations comparison to EU regulations

Side by side comparison of UK and EU regulations.

Management Systems

Learn about management systems compliant with ISO 13485 and UK MDR 2002.

UKCA Compliance Timelines

Find out how soon you need UKCA markings.