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AI assurance for healthcare
Assess, challenge and govern AI systems before they are embedded in patient care.
How it works
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Lawful

LENS helps organisations establish whether the use of an AI system is legally and ethically defensible before deployment.

LENS creates a clear record of the decisions made, the evidence relied upon and any actions required before the system is approved for use.

Explainable

​AI systems should be understandable enough for people to know what they are doing, what influences their outputs and where their limitations lie.

LENS develops SOP and training materials explaining:

  • how the system works in practice

  • what data, rules or models influence its outputs

  • known limitations and uncertainty

 

It creates a clear record of what the system does, how its outputs should be interpreted, and what people need to know before relying on it.

 

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Necessary

AI should only be used where it delivers a genuine benefit and is proportionate to the risks introduced.

LENS helps organisations assess:

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  • the intended benefits and who is expected to gain from them

  • whether the use is proportionate to the risks introduced

  • whether the system fits the clinical or operational context

  • whether continued use remains justified over time

 

It creates a clear record of why AI is being used, what benefit it is expected to deliver, and why that use remains proportionate.​

Safe

LENS clinical safety module supports your obligations.

The Clinical Safety module helps organisations manage:

  • DCB0160 clinical safety assurance

  • DCB0129 supplier clinical safety evidence

  • Clinical Safety Officer (CSO) review and sign-off

  • Clinical Risk Management Plans

  • Clinical Safety Cases and Clinical Safety Case Reports

  • Hazard Logs

  • clinical risk assessment and residual risk

  • safety controls and mitigations

  • clinical safety incidents

  • supplier safety evidence

  • local deployment and implementation risks

  • ongoing clinical safety monitoring and review

 

LENS creates a structured, auditable record of clinical hazards, controls, evidence, decisions and residual risk, supporting safer deployment of digital health technologies in NHS primary care.

 

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How it works
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