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RequestUpdated on 15 June 2026

Seeking input on NHS pilot-readiness evidence

Founder, CEO at NEUVIOR® - UK Pharma Infrastructure

London, United Kingdom

About

I’m looking for practical input from people who understand regulated innovation, NHS adoption, clinical safety, standards, AI assurance, procurement, evidence generation or healthtech commercialisation.

The question I’m working through is:

What evidence makes staff-facing medicines workflow software credible before a controlled NHS pilot?

Specific input I would value:

• intended-use wording
• safe product boundary
• source provenance expectations
• medicines identity and terminology risks
• standards language
• DCB0129/DCB0160 readiness thinking
• DTAC evidence planning
• IG, DPIA and data minimisation route
• AI governance and human review
• procurement route
• pilot evaluation metrics
• what NHS innovation teams actually trust

This is not a request for endorsement. It is a request for honest, practical challenge from people who can help make the pilot route safer, clearer and more credible.

Organisation

NEUVIOR® - UK Pharma Infrastructure

Businesses

London, United Kingdom

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