MHRA Compliance

At Gi-Cognition Ltd, we are committed to maintaining the highest standards of quality, safety, and regulatory compliance in everything we do. As part of this commitment, we are fully registered with the UK Medicines and Healthcare products Regulatory Agency (MHRA) for the manufacture and distribution of in vitro diagnostic (IVD) devices.

Our Registration

Gi-Cognition Ltd is officially registered with the MHRA as a manufacturer of IVD devices in accordance with UK medical device regulations.

• MHRA Manufacturer Register:
  View our listing

• MHRA Device Register:
  View our devices

These listings confirm our compliance with UK law for companies involved in the production, labelling, and supply of IVD medical devices used for clinical diagnostics, including tests processed at home and in clinic.

What This Means for You

Being MHRA-registered ensures that:

• Our in vitro diagnostic devices (IVDs) meet UK regulatory standards

• Our products are manufactured under quality-assured processes

• We operate with accountability and transparency in the healthcare sector

Whether you’re a patient, clinician, or partner organisation, you can be confident that all devices and test kits from Gi-Cognition Ltd are developed in line with recognised medical safety guidelines.

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For more information about our products, test kits, or regulatory documentation, feel free to contact us:

📧 ad***@**********on.com
📞 +44 (0)203 411 2011